Showing posts with label bacteria. Show all posts
Showing posts with label bacteria. Show all posts

Tuesday, June 7, 2011

"E. coli O104:H4--A Biochemist Offers Alternative & Natural Treatments For STEC: Do You Have A Question?" By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"

 Dear Ones:
     If you would like a particular subject addressed in my upcoming article on 'Natural Treatments For The Current E. coli STEC O104:H4 Outbreak', please email me at BarbaraKSexton@aol.com
     Health Care Providers may also request a consult.
God Bless & Keep Us At This Time
Reverend Barbara Sexton
"The Biblical Biochemist-Where Science Meets the Cross"

Thursday, June 2, 2011

"STEC O104:H4 E. coli Outbreak In Europe: eCDC Stats For June 2, 2011 & What They Mean For You & Your Family" By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"

eCDC Headquarters 'Tomteboda' http://www.ecdc.europa.eu/en/Pages/home.aspx
 Dear Readers:
      The eCDC (The European Center For Disease Prevention And Control) has published some new statistics today related to the recent E.coli STEC O104:H4 outbreak attributed to contaminated 'raw vegetables', including cucumbers, tomatoes and lettuce.
      Please exercise care when listening to 'headlines' regarding the number of deaths and illnesses allegedly taking place.
      Make no mistake: this is a horrible infection which is spread very easily and it is deadly.
     However, at the present time, the eCDC, the U.S. CDC and the individual health agencies of the European states are AT ODDS WITH EACH OTHER when it comes to 'NUMBERS of DEATHS and ILLNESS'.
     For background information, be sure to also read the FIRST in my series of articles, for you so that you and your loved ones may be safe during this food crisis: 
LINK: http://dearoneshealingministry.blogspot.com/2011/06/e-coli-outbreak-in-europe-stec-0104h4.html
     It is important to not PANIC in Europe or elsewhere at this time, but do exercise proper food-preparation precautions, and, for now, AVOID ANY AND ALL FOODSTUFFS IMPLICATED IN THIS RECENT STEC O104:H4 OUTBREAK!
     Remember that it is the 'SHIGA-Type Toxin' which causes death and tissue destruction with this STEC O104:H4 outbreak and this toxin cannot be washed away.
     Also, it is impossible to totally disinfect (i.e. wash with soap and water or with water and chlorine) foods such as vegetables.
     Thus, unfortunately for now, the only way to avoid becoming infected with this E. coli species is to AVOID ALL FOODS REPORTED TO BE CONTAMINATED IN EUROPE.
     For those in the U.S., I urge that you maintain a 'high index of suspicion' with fresh vegetables until and unless the situation in Europe is better understood and dealt with.
     Until then, we pray for those at risk at this time that they be safe and be made well.
     Since this is 'reportedly' a strain 'hitherto unseen until now' (which is true outside of academic circles), then the possibility of bioterrorism must be addressed at once by officials!
     As long as 'experts' quibble amongst themselves, the consumer is at risk and must seek their own counsel. 
     If you suspect that you or your family exhibit sign/symptoms of E. coli food-borne disease, wherever you are in the world, get them to a proper health care provider immediately.
     Do not wait, especially with children and infants!
     While this bacteria species is difficult to 'kill', supportive care can be provided and lives saved.
     Remember to keep an eye out for: stomach pain, cramps, diarrhea-bloody or otherwise, nausea, vomiting, weakness, 'feeling sick all over', brain-fog, seizures, urinary/kidney pain and problems, bleeding anywhere, dehydration...and ACT IMMEDIATELY AND GET HELP!
     And be sure to check in here regularly as I attempt to provide you with the very latest advice and VERIFIABLE DATA related to the European STEC O104:H4 outbreak.
God Bless You
Reverend Barbara Sexton 
"The Biblical Biochemist-Where Science Meets the Cross"
www.DearOnesHealingMinistry.blogspot.com
LINK FOR ARTICLE BELOW:
 http://www.ecdc.europa.eu/en/activities/sciadvice/Lists/ECDC%20Reviews/ECDC_DispForm.aspx?List=512ff74f-77d4-4ad8-b6d6-bf0f23083f30&ID=1096&RootFolder=%2Fen%2Factivities%2Fsciadvice%2FLists%2FECDC%20Reviews



Outbreak of Shiga toxin-producing E. coli in Germany
Epidemiological update, 2 June 2011, 11:00
On 22 May, Germany reported a significant increase in the number of patients with haemolytic uremic syndrome (HUS) and bloody diarrhoea caused by Shiga toxin-producing E. coli (STEC).
Since 2 May 2011, 499 cases of HUS have been reported from European Union Member States, including 470 cases in Germany. See table below.
While HUS, caused by STEC infections, is usually observed in children under 5 years of age, in this outbreak the great majority of cases are adults, with more than two thirds being women. Ten of the HUS cases have died.
Laboratory results indicate that STEC serogroup O104:H4 (Stx2-positve, eae-negative, hly-negative, ESBL, aat, aggR, aap) is the causative agent. PFGE results shows indistinguishable pattern of 7 human O104:H4 outbreak strains in Germany and 2 strains of O104:H4 in Denmark.
The source of the outbreak is under investigation, but contaminated food seems the most likely vehicle of infection. There is currently no indication that raw milk or meat is associated with the outbreak.
Most cases are from, or have a history of travel to the North of Germany (mainly Schleswig-Holstein, Lower Saxony, North-Rhine-Westphalia and Hamburg). Within the EU, Sweden, United Kingdom, the Netherlands, Denmark and Spain have reported cases of HUS, related to the ongoing outbreak.
Number of HUS cases and associated deaths per EU Member States as of 2 June 2011, 11:00

Member States Number of HUS cases Number of death associated
Countries reporting cases
Denmark 7 0
Germany 470 9
Sweden 15 1
The Netherlands 4 0
The United Kingdom 2 0
Spain  1 0

Based on the available information, cases are associated with an exposure in Germany (mainly northern parts). The vehicle of the outbreak has not yet been identified and intensive investigations are ongoing. The results of these investigations will determine the assessment of this risk. Rapid identification of potential cases linked to this outbreak, within Germany or among persons who have travelled to Germany since the beginning of May, is essential to prevent the development of severe disease.
STEC is a group of pathogenic Escherichia coli (E. coli) strains capable of producing Shiga toxins, with the potential to cause severe enteric and systemic disease in humans.
Read more
Escherichia coli (E.coli) health topic site: See ECDC risk assessment, list of all epidemiological updates, disease information

Wednesday, June 1, 2011

"E. coli Outbreak in Europe-STEC O104:H4-What It Means For You & Your Family" By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"

 courtesy: http://lci.tf1.fr/lexique/concombres-contamines-ce-qu-il-faut-savoir-6510062.html
UPDATE: 6/1/11  Be careful with what you hear on the news.  There are conflicting reports from various reporting agencies regarding either an increase or decrease in numbers of deaths and illness in the form of HUS from STEC O104:H4.  Reports thus far have been from 'unidentified and/or unsubstantiated sources' (and in the case of two alleged U.S. deaths from 'unidentified state sources).  Rest assured that once verifiable scientific data is available, Rev. Barbara Sexton will provide you with LINKS and  the most accurate information possible, along with her unique 'translation of the biomedicalese' for those who wish to understand it all.  Stay tuned.
_________________________________________________________ 
Dear Readers:
     There is a serious situation in Europe today regarding a great number of illnesses and deaths attributed to an  E. coli bacteria.
     By now you've read enough to know that there are many specifics 'types' of  E. coli bacteria, some more infectious than others.  
     The strain under consideration here is extremely RARE and has not, to date, been found in the United States.
     A recent CDC statement can be found below, which I will break down for you as best as I can.
     Please also 'click on' keywords below of interest to you for additional articles I have written to help you keep yourselves and your families as healthy as you can be.
     Here are some points of communal importance for us all:
---The RKI below in Germany is the equivalent of the CDC in the U.S.
---The RKI has so far confirmed 6 deaths and 373 patients with hemolytic uremic syndrome, or (HUS) (kidney failure), a life-threatening complication of E. coli infections.  This number is subject to change and will likely increase at any time.
---Given the extremely contagious nature of this outbreak, it is more imperative than ever that all TSA Officers regularly change their gloves and maintain high standards of hygiene for themselves and for the passengers they 'serve'.
     Remember that a TSA Officer's shirt/sleeve/wrist/glove/arm contaminated with fecal matter after a under-the-belt 'pat down' of a person suffering with a STEC 0104:H4 infection can infect many more persons, not to mention the TSA Officer themselves and their own families.  Good sanitation WORKS!  
     Infants and young children who travel are at particular risk at this time, so parents you must be extra vigilant and assertive, especially as youngsters seem to be singled out more and more for 'hands on' inspection by the TSA!
---The strain in question is E. coli O104:H4 is also known as STEC.  'STEC' stands for 'Shiga toxin-producing E. coli'.
---Note that it is the TOXIN which does the most damage during severe infection with 'STEC' E. coli.
---Signs and symptoms of infection with  STEC O104:H4 are VERY obvious.  Even non-lethal cases present with severe cramps and bloody diarrhea with nausea and vomiting.  The patient will 'feel very sick'.  PARENTS: IF YOUR CHILD OR OTHER LOVED ONE HAS THE SLIGHTEST INDICATION OF HAVING CONTRACTED AN INFECTION OF THIS SORT, SEEK MEDICAL HELP IMMEDIATELY.  DO NOT DELAY.  Infants, children, the elderly, those with chronic medical conditions and those who are immuno-compromised are at particular risk of developing severe, life-threatening complications such as kidney failure ( hemolytic uremic syndrome aka HUS)
---The 'Shiga-toxin' produced by this food-borne bacteria does it's damage by literally destroying the mucosal lining of the intestines with attendant hemorrhaging which results in the so-called 'bloody diarrhea'.  This toxin destroys all other body tissues, as well.  If and when the infection overwhelms the body, major organ failure is induced and death is inevitable.
----Even 'non-life-threatening' STEC O104:H4 infections can result in severe anemia (lack of sufficient red blood cells), dehydration and other sequelae.  Weakness and a sense of debilitation can persist afterwards for a long time.
---All body fluids/substance (especially feces, blood, urine, vomit) of a person infected with STEC O104:H4 should be considered 'infectious'.
---Thus far, no cases of STEC O104:H4 are reported in the U.S.A., but with modern travel, it is entirely possible that this strain will make itself known here soon enough.  
     Remember that E. coli bacteria, whatever the 'type',  live in the intestines of warm-blooded vertebrates and are carried thus.  E. coli species and subspecies USED TO BE 'species-specific', meaning that cows had bovine E. coli, while humans only had human-type E. coli.  
     But things have changed and these strains can 'cross infect' and worse, different bacterial genuses hitherto thought to be UNABLE to 'conjugate and exchange genetic material' have done just THAT...ergo the emergence of 'superinfectious strains' like the E. coli O157:H7 the United States is familiar with.
---Just because no cases of STEC O104:H4 haven't been reported in the United States or in U.S. Service Members stationed in Germany does NOT mean that they will not be.  Be alert!  Stay aware.
---Remembering that initial outbreaks of E.coli disease years ago were linked to hamburger meat, bear in mind that subsequent outbreaks in the U.S. and elsewhere in the world have been linked to various fruits, vegetables and just about any edible foodstuffs.
---The initial reports implicate CUCUMBERS, lettuce and tomatoes in Germany, as the source of the STEC 0104:H4, but this does not necessarily mean that that is the sole source of the infection.
---Understand that much 'under reporting' is due to the fact that healthy individuals with relatively 'mild' cases of food-borne illness never see a physician or other health care provider, let alone 'get reported' in accordance with state and federal protocols.
---Be aware that given the fact that STEC O104:H4 is very rare and that it is suddenly the source of such major infection, there is the possibility of deliberate tampering with the food supply.
      Fortunately, it is possible to conduct epidemiological forensic work akin to DNA analysis and all types of 'fingerprinting' on these microbes, not that the public will ever necessarily know the truth if tampering is discovered in a limited outbreak.
---The above said, nature has no equal when it comes to rapid development and spread of contagion, especially in the modern world with long-distance travel of persons, produce and products, traditional overuse of antimicrobials, depressions of immune systems due to environmental factors and medical intervention and human frailties.
     Finally, I once again urge that you all maintain HIGH PERSONAL HYGIENE STANDARDS.
     Carry antimicrobial gel with you and use it constantly.  Teach children to do the same.
     Remember that a flushing toilet 'shoots' an aerosolized mist a good six feet into the room, at least.  Store toothbrushes and personal care items well away from and/or protected from toilet 'spray'.
     Keep hands and fingers away from the face, out of the mouth/nose/eyes/ears, etc.
     Thoroughly wash ALL produce with a small amount of dish detergent and water and scrub with a vegetable brush.  Of course, be sure to rinse away all trace of 'soap smell'.
     I do not recommend the regular use of a bleach solution to disinfect food, unless sanitation conditions are at an all-time low.
     Certain foods such as lettuce and berries cannot be washed clean enough to be safe to eat if they are, indeed, contaminated with a pathogenic microbe such as those discussed here.
     Try to buy from reputable sources and organic if you can afford it.  But understand that eating tainted food is always a possibility under the best of conditions.
     Do note that even if ALL BACTERIA and other microbes are removed or killed before eating, TOXINS can STILL BE PRESENT which cannot be 'cooked or cleaned away'.
     It is better to 'do without' when in doubt, rather than risk your health and that of your family.
     That's it for now and be sure to check www.DearOnesHealingMinistry.blogspot.com regularly for updates as this situation with STEC O104:H4 unfolds.
     If you'd like to sign up for my FREE NEWSLETTER and get my latest news right in your mailbox, sign up below.
     Please be careful in this age of 'superbugs'.
May God Bless & Keep You
Reverend Barbara Sexton
"The Biblical Biochemist-Where Science Meets the Cross"
www.DearOnesHealingMinistry.blogspot.com
Questions/Comments: down below or email Rev. Barb at BarbaraKSexton@aol.com 
LINK for article below:  http://www.cdc.gov/media/releases/2011/s0601_ecoligermany.html?s_cid=2011_s0601_ecoligermany
CDC Statement on Outbreak of STEC O104:H4 infections in Germany
CDC is following a large outbreak of Shiga toxin-producing E. coli O104, or STEC O104, infections currently going on in Germany. As of May 31, 2011, the Robert Koch Institute (RKI), Germany's disease control and prevention agency, has confirmed six deaths and 373 patients with hemolytic uremic syndrome, or (HUS) (kidney failure), a life-threatening complication of E. coli infections.
To date, no confirmed cases of STEC O104 infections have been reported in U.S. travelers to Europe. Two cases of HUS in the United States have been reported in persons with recent travel to Hamburg, Germany. CDC is working with state health departments to learn more about these two cases and to identify others. CDC has been in contact with the German public health authorities at RKI. We have alerted state health departments in the United States of the ongoing outbreak. We have also requested that they report to CDC any cases in which people have either HUS or Shiga toxin-positive diarrheal illness, with illness onset during or after travel to Germany since April 1, 2011.
The strain of STEC causing illness, STEC O104:H4, is very rare. CDC is not aware of any cases of STEC O104:H4 infection ever being reported in United States. Any person with recent travel to Germany with signs or symptoms of STEC infection or HUS, should seek medical care and let the medical provider know about the outbreak of STEC infections in Germany and the importance of being tested. Symptoms of STEC infection include severe stomach cramps, diarrhea, which is often bloody, and vomiting. If there is fever, it usually is not very high. Most people get better within 5–7 days, but some patients go on to develop HUS—usually about a week after the diarrhea starts. Symptoms of HUS include decreased frequency of urination, feeling very tired, and losing pink color to skin and membranes due to anemia.
CDC is not aware that a specific food has been confirmed as the source of the infections. Travelers to Germany should be aware that the German public health authorities have recommended against eating raw lettuce, tomatoes or cucumbers, particularly in the northern states of Germany (Hamburg, Bremen, Lower Saxony, Schleswig Holstein). We have no information that any of these suspected foods have been shipped from Europe to the United States at this time. The US Department of Defense has been notified of this outbreak because of the presence of U.S. military bases in Germany. We are not aware of any cases among U.S. military personnel.
Here are answers to frequently asked questions:
  1. Would this be the largest E. coli outbreak ever in the world?

    We are still learning more about the overall size of this outbreak. The number of HUS cases involved indicates that the outbreak is very large.
  2. Tell us about this rare strain and are we testing for it here?

    A very rare strain of Shiga toxin-producing E. coli, or STEC has been reported from some patients in the outbreak. This strain, E. coli O104:H4 has never been seen in the United States, and CDC is only aware of few reports of this strain from other countries. Although it is rare, the United States' public health surveillance systems are designed to be able to identify this, and other rare STEC strains, in ill people. However, the ability to detect STEC infections through surveillance depends on proper diagnostic testing of patients presenting with symptoms suggestive of STEC. In 2009, CDC published recommendations for the diagnosis of STEC infections by clinical laboratories. The illness that it causes is similar to that caused by E. coli O157:H7 which is also a Shiga toxin-producing E. coli and the one most commonly identified in the United States.
  3. Could people travel from Germany and spread it here?

    STEC infections can be spread from person to person. The best defense is careful, thorough hand washing. Persons returning from Germany who have diarrhea should be sure to wash hands well with soap and warm water after using the bathroom, and should not prepare food for others while they are ill. People who are in contact with ill people who recently visited Germany should also follow basic hygiene practices carefully, including washing their hands thoroughly before eating or drinking and after caring for an ill person.
  4. Why so many sick people?

    It is too early to know why this is such a large outbreak. The large size may have to do with contamination of a popular food item. However, to our knowledge a specific food vehicle has yet to be confirmed. It is also possible that the unusual strain is particularly likely to cause HUS. 

Friday, March 25, 2011

"UPDATE: A Biochemist's Comprehensive INTERNATIONAL LIST Of Triad Alcohol Products Recalled By FDA Due To Bacterial Contamination Concerns" By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"

Some of the Triad (H & P Industries) Alcohol products recalled due to bacterial contamination
Dear Ones:
     Herewith is an updated international list of all the 'brand names' of TRIAD aka H & P Industries ALCOHOL PADS, SWABS and SWABSTICKS potentially contaminated with Bacillus cereus as of 3/25/11.
     This recall affects Canada, the US and Europe.
     Please check and see if the alcohol prep pads, swabs and swabsticks you may have in your possession have any of the brand names here and DO NOT USE THEM!
Allegiance
Best Choice
Boca
Care One
Conzellin
Cooper Atkins
CVS
Discount Drug Mart
Equaline
Equate
Exchange Select
Exact
Good Neighbor
Good Sense
Healthcare
Healthy Generations
Jean Coutu
Katz Group
Kroger
Leader
Life Brand
Loblaw
Longs
Major
MEIJER
Medicine Shoppe
Moore Medical
Personelle
PharmaChoice
PharmaPlus
Premier Value
PSS Select 
Publix
Premier Value
Quality Choice
Rite Aid
Reli-On
Remedy RX
Rexall
Safeway
Shoppers Drug
Shoppers Drug Mart 
Sunmark Top Care
Triad
Triad Sterile
Ultilet
Uniprix
Up&Up
Valu Plus
VersaPro
Western Family
Walgreens
     Read Triad's (H & P Industries) letter here:
LINK: http://www.triad-group.net/media/pdf/Recal_Facts.pdf

     And this is the FDA LINK for injectable kits affected by this Triad FDA Recall.
     Is your drug listed? (see highlights below)
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm239319.htm
Triad Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks: Recall Due to Potential Microbial Contamination

[UPDATED 03/23/2011] Eli Lilly and Company notified customers not to use Prep Pads in black starter kits for Forteo [teriparatide (rDNA origin) injection].
[UPDATED 03/09/2011] Smith & Nephew issued a recall of IV PREP Antiseptic Wipes, manufactured for Smith & Nephew by The Triad Group.
[UPDATED 02/11/2011] Triad Alcohol Prep Pads are packaged with devices manufactured by Neuro Resource Group. The Triad alcohol prep pads should not be used.
[UPDATED 02/07/2011] Triad Alcohol Prep Pads are a component of Extavia (interferon beta 1-b) packaging marketed by Novartis. The Triad alcohol prep pads should not be used.
[UPDATED 02/05/2011] Triad Alcohol Prep Pads are a component of a convenience kit distributed with Watson’s Trelstar (triptorelin pamoate for injectable suspension) product. The Triad alcohol prep pads should not be used.
[UPDATED 02/01/2011] FDA reminded healthcare professionals about the safe use of non-sterile alcohol prep pads to clean and disinfect the surface of the skin.
[UPDATED 01/28/2011] Triad Alcohol Prep Pads may have been included in U.S. packaging for Arixtra Starter Kits manufactured by GlaxoSmithKline (GSK). The Triad alcohol prep pads should not be used.
[UPDATED 01/26/2011] Triad Alcohol Prep Pads are packaged for use with the kit presentation of Relistor (methylnaltrexone bromide) Subcutaneous Injection in the U.S. The Relistor vial and other components of the kit are not affected by the defective Triad alcohol pad. Relistor sold in single vials also is unaffected by this recall. Pfizer and Progenics advise patients using the Relistor kit not to use the Triad alcohol prep pads included in the Relistor packaging for 1 X 7 kits and 1 X 2 starter kits. When preparing to take their Relistor injection, patients should use an alcohol prep pad from a company other than Triad, or use a sterile gauze pad with isopropyl alcohol.
[UPDATED 01/21/2011] Triad alcohol prep pads packaged for use in the U.S. with Betaseron (interferon beta 1-b) should not be used by patients. There is no involvement or potential contamination of the Betaseron vial or other components in the Betaseron U.S. packaging. This issue is confined to the actual Triad alcohol prep products. Triad alcohol prep products are not used in Betaseron packaging outside of the United States. Bayer has halted shipments of Betaseron to its distribution network, until it can affect a replacement for the alcohol prep pad.
Bayer is instructing patients using Betaseron to immediately discontinue using the Triad alcohol prep pads included in the Betaseron packaging and dispose of those pads in the trash. When preparing to take their Betaseron injection, patients should use an alternative alcohol prep pad that is not subject to this Triad recall or use a sterile gauze pad in conjunction with isopropyl alcohol.
[UPDATED 01/14/2011] The Triad Group alcohol prep pads are co-packaged and distributed with Genentech medicines Boniva Injection, Fuzeon, Nutropin A.Q.Pen, Pegasys, and TNKase to customers in the United States. Genentech medicines are not contaminated and may continue to be used in accordance with the package insert. Patients and healthcare providers should not use the alcohol prep pads packaged with these medicines and should instead use an alternate alcohol prep pad that is not involved with the Triad Group recall.
God Bless You
Reverend Barbara Sexton
"The Biblical Biochemist-Where Science Meets the Cross"
http://www.dearoneshealingministry.blogspot.com/

Saturday, March 12, 2011

"Triad 'Sterile' Lube Jelly FDA Recall Affects Australia, Belgium, Canada, China, Lebanon, New Zealand, Philippines, Northern Marianna Islands, Saudi Arabia, Singapore, Taiwan, and United Arab Emirates As Well As The U.S.A." By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"

Triad 'Sterile' Lube Jelly
Dear Global Readers:
     The Triad 'Sterile' Lube Jelly FDA Recall affects many all across the globe, as listed below:
"Worldwide distribution: USA including states of: CA, CO, CT, FL, GA, IL, IN, KS, KY, LA, MA, MI, MO, MS, MY, NC, NE, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, VA, WA, WI and Puerto Rico; and countries including: Australia, Belgium, Canada, China, Lebanon, New Zealand, Philippines, Northern Marianna Islands, Saudi Arabia, Singapore, Taiwan, and United Arab Emirates."
LINK:
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/resCollection_2.cfm?ID=96796&CREATE_DT=2011-01-21
     Brand Names affected include:
     Allegiance
     Cardinal Health
     Select Medical Products
     PSS World Medical, Inc.
     Novaplus
     Novation, Inc.
     Triad
     Triad Plus
     Triad Group, Inc.
     IMCO
     Independent Medical Co-op, Inc.
     McKesson Medi-Pak
     Performance
     McKesson Corporation,
     McKesson Surgical
     Henry Schein
     PLEASE BE SURE TO READ MY CONSTANTLY UPDATED 'TRIAD' PAGE WITH A LIST OF ALL THE ARTICLES I HAVE WRITTEN ON RECALLS OF TRIAD'S ALCOHOL AND 'STERILE' LUBE JELLY PRODUCTS.
     Here's the TRIAD PAGE LINK:
http://dearoneshealingministry.blogspot.com/p/triad-alc-pad-fda-recall.html
God Bless You
Reverend Barbara Sexton
"The Biblical Biochemist-Where Science Meets the Cross"
http://www.dearoneshealingministry.blogspot.com/

"Unhappy With Your Liposuction Results As Far Back As 2004?-Read Here About A Possible Triad 'Sterile' Jelly Connection" By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"


Dear Ones:
     The Triad Alcohol prep pads and swabs and Triad 'Sterile' jelly lube story will just not go away.
     I recently came across a MAUDE Report (Manufacturer and User Facility Device Experience Database) implicating Triad 'Sterile' Jelly Lube in a number of unsatisfactory liposuction results.
      The MAUDE Report is dated 2004, but the page it is on was recently UPDATED on Feb. 28, 2011.
"THE TRIAD GROUP, DIVISION OF H & P INDUSTRIES TRIAD LUBRICATION JELLY LINK: http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=611249 
Event Date 06/01/2004  Event Description:
There is an urgent need for fda to investigate a product that is currently being used by plastic surgeons during liposuction procedures that is creating tremendous wound problems that have never been seen before. Between one hundred to two hundred pts have been adversely affected with scarring and infected foreign body reactions from the use of a lubrication jelly produced by triad. The use of triad lubrication jelly started in june 2004 when the johnson and johnson k-y jelly was discontinued. The local distributors substituted the triad brand lubrication jelly. The jelly is used during the liposuction procedure to keep the wound edges from being traumatized by the metal liposuction cannula that moves in and out of the wound several hundred times at a quick pace. Most plastic surgeons started noticing unusual wound healing problems around the incision sites that typically healed without any problems. The healing problems started with severe redness and induration followed by opening of the wound at 2-4 months and chronic drainage with cellulitis in many cases. In all cases the resulting scarring is far worse than the normal small line that forms after liposuction. In dec 2004 a group of plastic surgeons who use the same surgical facility came to the conclusion that the triad gel was the only factor in their procedures that had been changed. This particular group started contacting other plastic surgeons in the ensuring months and several other surgeons reported similar problems in every liposuction pt where the triad jelly was used. At plastic surgery meetings more and more surgeons were reporting this wound healing problem with the only common factor being the triad jelly. Triad was initially contacted by a physician in dec. 2004, but no letters or measures were taken to notify physicians or distributors about the potential problems in using jelly during liposuction. In feb. Of 2005 an official letter from triad was released by their quality control division stating that the jelly had successfully passed all the necessary quality controls and that the triad jelly was similar to other equivalent jelly being used in the market place. Again no letter was issued to physicians or the distributor of the product about the potential problem with this type of usage. There is a list of board certified plastic surgeons who have used triad jelly and have numerous pts in their practices with ongoing wound and scar problems. Reporter has been contacted by pt's attorneys as well as several other physicians who have pending law suits based on infections and scarring. Fda should open an immediate investigation and in the very least have triad circulate a warning to all physicians and distributors of the product. The physicians are willing to cooperate in any way to assist the fda in collecting info in a timely fashion."
     Perhaps this information will be of some help to you.
With Love in Christ
Reverend Barbara Sexton
"The Biblical Biochemist-Where Science Meets the Cross"
www.DearOnesHealingMinistry.blogspot.com 

Triad Sterile Lubricating Jelly

Monday, March 7, 2011

"Triad Sterile Lube Not So Sterile-Just Like Triad Alcohol Products: Check Your Brand Here" By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"

Triad Not-So 'Sterile' Lubricating Jelly
Dear Ones:
         Once in a while we come across a 'recall situation' that is so NOT forth-coming and disclosive that it fairly begs for continued, intense scrutiny.
     Such is the case with Triad Products.
     My main focus of concern at this time is Triad's 'Sterile Jelly' Recall, which received very little press to date, but which demands greater scrutiny now, in my opinion.
      Just for the record, here is their company 'recall page':
LINK: http://www.triad-group.net/index.php?option=com_content&view=section&layout=blog&id=1&Itemid=58
     And here is the link for all FDA notices related to 'Triad Group Recalls':
LINK: http://google2.fda.gov/search?q=triad+group+recalls&client=FDAgov&site=FDAgov&lr=&proxystylesheet=FDAgov&output=xml_no_dtd&getfields=*&x=8&y=13
     (If you use the above, be sure to 'refresh' the search tool embedded in it.)
     The Triad lube jelly link is dated way back to this past December 23, 2010
LINK: http://www.fda.gov/MedicalDevices/Safety/RecallsCorrectionsRemovals/ListofRecalls/ucm243399.htm       Triad's so-called 'sterile lube jelly' is used to lubricate everything from catheters to fingers, endoscopes and other medical instruments.
     BRANDS AFFECTED BY TRIAD'S STERILE LUBE JELLY RECALL:
     According to Triad, itself, the following 'brand names' are involved in this lube jelly recall:
Triad
Cardinal
Novation
McKesson
Imco
Select
Schein
     A cursory examination of Triad's 'products recall page' reveals that the company is not very 'forthcoming' with information, except to identify the products involved:
Triad Group, Triad Sterile Lubricating Jelly

Recall Class: Class II
Date Recall Initiated: December 23, 2010
Products: Sterile Lubricating Jelly, packaged in:
5 gram tubes
2 ounce and 4 ounce tubes
4 ounce bottles
3 and 5 gram packets
This recall affects all Triad lubricating jelly packages with lot numbers beginning with the numbers 7, 8, 9, or 0. If these packages are part of kits, packs, or trays, the lot numbers will only appear on the lubricating jelly packages.
The Triad lubricating jelly products were distributed by Triad from January, 2007 through December 2010. These products may be contained in kits, packs, or trays that have been packaged after December 2010 by other firms.
FDA will update this webpage when additional information is available.
The following table provides brand names, distributors, and product identifiers (catalog or reorder numbers) known at present:
BRAND NAMES FIRM NAMES CATALOG/
REORDER #s PRODUCTS
Allegiance Cardinal Health LJT2
LJF3
LJT4
LJT5 Net Wt. 2 oz.
Net Wt. 3g
Net Wt. 4 oz.
Net Wt. 5g
Select Medical Products PSS World Medical, Inc. 137
136 3g/packet
4 oz.
Novaplus Novation, Inc. V10-8344
V10-8919
V10-8917 Net Wt. 3g
Net Wt. 4 oz.
Net Wt. 2 oz.
Triad
Triad Plus Triad Group, Inc. 10-8917
10-8946
11-8344
11-8472
10-8919
10-8500 Net Wt. 2 oz.
Net Wt. 5g
Net Wt. 3g
Net Wt. 5g
Net Wt. 4 oz.
Net Wt. 4 oz.
IMCO Independent Medical Co-op, Inc. 8919-IMC Net Wt. 4 oz.
McKesson Medi-Pak
Performance McKesson Corporation,
McKesson Surgical 66-8919 Net Wt. 4 oz.
Henry Schein Henry Schein, Inc. 104-9637 Net Wt. 4 fl. oz.
Under Useful Links below, see also firm recall letter and recall webpage, related FDA News Release on non-sterile alcohol prep pads, and related firm Press Releaseon Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks.
Use: This product helps to provide easy insertion of a medical device (such as a catheter or an endoscope) or gloved fingers into body openings.

Recalling Firm:
H & P Industries, Inc., doing business as, Triad Group
700 West North Shore Drive
Hartland, Wisconsin 53029-8358
Reason for Recall: This product may not be sterile. Patients, who are immuno-compromised, such as those with diabetes, cancer and certain other chronic diseases, may be at potential risk for infection.
Public Contact: Customers with questions may contact Triad Group Customer Service at 1-262-538-2900 ext. 2761, Monday through Friday, from 8:30 AM through 4:00 PM, Central Time or your distributor.
FDA District: Minneapolis
FDA Comments:
On December 22, 2010, the company sent an “Urgent Medical Device Recall” letter to all its customers by certified mail. The letter described the issue, identified the affected products with the lot numbers beginning with the digits 7, 8, 9, or 0, as well as the action to be taken by the customers.
Triad Customers (Distributors, and kits, packs, or trays’ manufacturers) were instructed to:
IMMEDIATELY EXAMINE their inventory.
QUARANTINE only lubricating jelly products.
IMMEDIATELY NOTIFY their customers if the recalled product was further distributed.
COMPLETE AND RETURN the enclosed Recall Acknowledgement form by FAX at 1-262-538-2947 or mail to: Recall Coordinator, Triad Group, 700 West North Shore Drive, Harland, Wisconsin 53029, OR
RETURN the recalled product to the appropriate company, if not the Triad Group.
Additional Information:
Triad sterile lubricating jelly products have been incorporated into a variety of procedural and convenience kits, packs, or trays with other medical devices and/or drug products.
Healthcare facilities: IMMEDIATELY CONTACT your kit, pack or tray suppliers to determine whether the products stocked at your facility are impacted by the Triad recall. Your supplier should provide you with documentation on whether your products are affected by the recall.
FDA is instructing manufacturers and repackers who have incorporated the recalled products into their kits, packs or tray to PROMPTLY CONDUCT A SUB-RECALL and submit their recall strategies to their FDA District Office.
Health care professionals and consumers may report adverse reactions or quality problems they experienced using these products to FDA’s MedWatch Safety Information and Adverse Event Reporting Program1 either online, by regular mail or by FAX.
Useful Links:
Triad Recall Letter 23
Triad Recall Webpage4 5
FDA News Release - Safe Use of Non-Sterile Alcohol Prep Pads 6
Firm Press Release on Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks 7  
Foley Catheters which require the use of a 'sterile lubricating gel'
      We get a somewhat better 'handle' on what may be going on with Triad's lube jelly by reading it's "URGENT MEDICAL RECALL LETTER" dated last Dec. 22, 2010:
"This is to inform you of a product recall involving Sterile Lubricating Jelly distributed by Triad Group. This recall has been initiated due to concerns expressed by the Food and Drug Administration regarding the validation of the gamma radiation sterilization cycles for these products. We are initiating this recall because use of inadequately sterilized product might result in patient infection.
LINK: http://www.triad-group.net/media/pdf/LJ_Recall_Ltr_FINAL.pdf
     That which is highlighted above is quite an understatement, since Triad products have been implicated in a number of very serious Bacillus cereus infections (see alcohol pads, swabs and swabstick articles.)
     But, to date, we can find scant information on exactly what kind of 'contamination' affects the recalled Triad lube jelly.

     My advice to you, dear Readers, is to REFRAIN FROM USING TRIAD PRODUCTS, since clearly The Triad Group has a number of 'sterilization issues' with a number of it's products.
     Until more information is released by both Triad, itself, the FDA, private laboratories and third-party witnesses and 'discoverers', it is wise to be cautious.
     Do not depend upon either a commercial manufacturer NOR a government agency to look out for your health!
     Check back here regularly to read the latest.  Just click on the 'Triad Page' on the right.
     Or better yet, sign up to receive Rev. Barb's FREE HEALTH NEWSLETTER.  See details at page bottom.
     And, as always, consult with your personal health care advisor to get the very best input on protecting your health and that of your loved ones.
Blessings,
Reverend Barbara Sexton
"The Biblical Biochemist-Where Science Meets the Cross"
www.DearOnesHealingMinistry.blogspot.com

Thursday, February 17, 2011

"Triad Alcohol Swabs Implicated In Houston Toddler's Meningitis Death" By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"


LINK:
Triad Alcohol Products-prep pads, swabs & swabsticks
Dear Ones:
     I've been praying something like this would not have to be written. 
     But there is a possibility that a Houston toddler died as a result of Triad alcohol prep products being used on his recent lumbar surgical incision area after cyst removal surgery.
     And it is, in fact, the tragic story of this youngster Harrison Kothari which may have been the case that triggered the Triad alcohol prep pad and swabstick RECALL I've been writing about here on this blog since January 20, 2011.
     Note: LINKS below are listed chronologically:
LINK: http://dearoneshealingministry.blogspot.com/2011/01/contaminated-alcohol-swabs-recalled-in.html
     Here are some additional follow-up articles:
LINK: http://dearoneshealingministry.blogspot.com/2011/01/genentechinjectables-boniva-fuzeon.html
LINK: http://dearoneshealingministry.blogspot.com/2011/01/now-pfizer-progenics-recalling-relistor.html
LINK: http://dearoneshealingministry.blogspot.com/2011/02/neuro-resource-group-issues-recall-due.html
     Below are the heart-wrenching details of the ordeal parents Sandra and Shanoop Kothari went through with their two year old son Harrison:-
----------------------------------------------------------------------------------------------
Company recalls alcohol swabs after Houston toddler's meningitis death "by Leigh Frillici and Courtney Zubowski / 11 News
www.khou.com 
Posted on February 14, 2011 at 6:17 PM
Updated Monday, Feb 14 at 10:46 PM
HOUSTON—Looking at the pictures of 2-year-old Harrison Kothari in his family’s home, you see a smiling, laughing child.
What you’d never know is the little boy had brain surgery a month earlier to remove a benign cyst.
"He was a happy, beautiful 2-year-old boy," said Sandra Kothari, Harrison’s mother. "He loved music, he loved playing with his 7-year-old sister."
Shortly after turning 2, Harrison died during his hospital stay at Children’s Memorial Hermann. At the time, he had a drain inserted in his spine to remove some fluid, and he was set to go home the next day.
"He had healed fabulously," said Shanoop Kothari, Harrison’s father. "He was going to get the drain removed the next day."
That night, the boy developed bacterial meningitis. He died hours later.
The Kotharis believe alcohol swabs made by TRIAD Group, Inc., were to blame. They say the swabs were used to clean their son’s drain. The Kotharis believe the swabs were contaminated with a nasty bacteria called bacillus cereus—more commonly known to cause food poisoning.
"In managing a lumbar drain, they use the swab on the portal," said Jim Perdue, the Kotharis attorney. "And so, it’s pushed in and pulled back out so there is literally an opportunity to have injected this bacillus cereus into the lumbar drain every time they used an alcohol swab."
Triad Group has voluntarily recalled all of its alcohol products. The company also makes alcohol pads and swabs for dozens of other stores, like CVS, Kroger, Safeway and Walgreens.
Perdue says the concerns aren’t just for patients like Harrison, but also for people who use Triad alcohol pads for injections.
They are suing the company."
"It’s a very resistant bacteria (bacillus cereus)," said Perdue. "The body is able to fight it off if you have a healthy person. But when you’re talking about injections for people with M.S. or diabetes and they’re literally using this at the injection site and then puncturing the skin, it can cause some really serious problems."
Houston endocrinologist Dr. Eric Orzeck said if there was in fact contamination, the very young that don’t have as strong as an immune system are particularly at risk.
"When it’s applied to the skin and there’s an open area in which you would use when you’re getting an IV, that can cause a very severe local infection," said Dr. Orzeck.
He says symptoms could develop within 24 hours of using it.  Those who haven’t seen symptoms past two days are probably OK, Orzeck said.
There are several symptoms the doctor says to keep in mind.
"It might be headaches or difficulty breathing, obviously infection at the site which would be apparent with redness and swelling," he said.
What concerns the Khotaris is that most people haven’t heard of the recall.
"People could have these in their homes, in their bathrooms right now," said Sandra Kothari.
And so as painful as it is to talk about their son, the Kotharis hope that people will remember their little boy and do a simple thing—check their medicine cabinets.
Children’s Memorial Hermann Hospital released a statement in response to the tragic news.
"Children’s Memorial Hermann Hospital is deeply saddened by the death of any child in our care," it read. "Memorial Hermann was notified of the product recall in January, one month after this child died. At that time, the product was removed from our shelves. We are dedicated to providing the highest standard of quality care and patient safety at Children’s Memorial Hermann Hospital."
The manufacturer has not responded to an 11 News request for information, but its website states:
"This recall has been initiated due to concerns from a customer about potential contamination of the products with an objectionable organism that may or may not be related to Triad’s manufacture of these products. We are, out of an abundance of caution, recalling these lots and revalidating our production lines…"
LINK: http://www.khou.com/news/local/Company-recalls-alcohol-swabs-after-toddlers-meningitis-death-116197699.html 
-----------------------------------------------------------------------------------------------
     If you haven't already, you may want to sign up for my FREE NEWSLETTER and get the latest news 'explained' and sent right to your email box.  See details below.
     Please have a 'care and a prayer' for this poor grieving Kothari family as we continue to stay on top of the Triad alcohol product FDA Recall.
     And pray for those who manufacture Triad products and for those who manufacture products co-packaged with Triad brand alcohol products.
     It is a worst fear and a nightmare to know that one may be inadvertently, partly or even completely responsible for a tragedy such as the loss of little Harrison Kothari.
God Grant You His Blessings
Reverend Barbara Sexton
"The Biblical Biochemist-Where Science Meets the Cross"
www.DearOnesHealingMinistry.blogspot.com



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"Neuro Resource Group Issues Recall Due To Potentially Contaminated Triad Alcohol Prep Products" By Reverend Barbara Sexton "The Biblical Biochemist-Where Science Meets the Cross"

Dear Ones:
   Another company, Neuro Resource Group, has issued a recall of it's medical devices which are co-packaged with Triad brand alcohol prep pads, alcohol swabs and alchohol swabsticks.
     According to Neuro Resource Group's website:
"Neuro Resource Group (NRG) specializes in the development, design and manufacture of innovative medical products for injury management, rehabilitation, and pain management. The Company's management team has extensive experience in the healthcare industry and is committed to providing products and developing training materials and protocols that help to improve the quality of patient's lives and also enhance athletic performance on both a professional and non-professional level."
LINK: http://www.nrg-unlimited.com/index.php/about-nrg.html 
     NRG's medical devices for CONSUMERS include:  
Single Patient Systems: A range of body specific Conductive Garments for home use and

Single Patient Systems: A range of body specific Conductive Garments for home use
(Health Care Professionals, see photos of Professional Devices below)
    
     It is important that everyone NOT USE any TRIAD ALCOHOL PREP PRODUCTS which can be identified by either “Triad Group,” listed as the manufacturer, or the products which are manufactured for a third party and use the names listed below in their packaging:
LINK: http://www.fda.gov/Safety/Recalls/ucm242736.htm
Cardinal Health
PSS Select
VersaPro
Boca/ Ultilet
Moore Medical
Walgreens
CVS
Conzellin
Select
Select Medical Products
PSS Select
PSS World Medical, Inc
     Please note that these Triad alcohol prep products were distributed in the UNITED STATES, CANADA and EUROPE.
     Below is the information on the FDA site:
Informs Customers of Important Information
about Triad Group's Alcohol Prep Pads
Contact:
Sarah Magee
972-665-1810 X231
FOR IMMEDIATE RELEASE - February 7, 2011 -Neuro Resource Group, Inc. (NRG) has become aware of the market recall of Triad Group's alcohol prep pads, alcohol swabs, and alcohol swabsticks manufactured by Triad in the United States and marketed under various brand names, http://www.fda.gov/Safety/Recalls/ucm239219.htm9 . The Triad Group alcohol prep pads are co-packaged and distributed with NRG devices to customers in the United States and internationally.


According to the Food and Drug Administration's (FDA) Medwatch communication, the recall was initiated due to concerns about potential contamination of the Triad Group's products with the bacteria, Bacillus cereus. This recall involves those products marked as sterile as well as non-sterile. Use of contaminated alcohol prep pads, alcohol swabs, and alcohol swabsticks could lead to life-threatening infections, especially in at-risk populations, including immune suppressed and surgical patients. The Triad wipes may also be labeled “Select”; “Select Medical Products”; “PSS Select”, or “PSS World Medical, Inc.” The subject Triad/Select alcohol wipes previously provided with NRG devices should be discarded immediately. NRG is currently providing alcohol wipes that are not subject to recall.


It is important to note, that NRG devices are not contaminated and may continue to be used in accordance with the instructions for use. The alcohol wipes were provided strictly as a cleaning convenience. Patients and healthcare providers should not use the Triad/Select alcohol prep pads packaged with these devices and should instead use an alternate alcohol prep pad that is not involved with the Triad Group recall, or alternatively use a gauze or tissue pad in conjunction with 70% isopropyl alcohol for cleaning. For replacement wipes, customers may contact NRG customer service at 1-877-314-6500.

The company plans to issue a letter to customers to make them aware of the Triad product recall and the need to discontinue use of the Triad alcohol prep pads packaged with NRG products. Further information about the Triad Group recall can be found on the FDA website at: http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm239319 .htm10.


Patients should consult their healthcare provider for further information. Healthcare providers with questions may contact NRG Customer Service at 1-877-314-6500 between the hours of 8 am and 5 pm Central Time."

     Please take care if you use these devices. DO NOT USE any TRIAD ALCOHOL PRODUCTS packaged with them.
God Bless You
Reverend Barbara Sexton
"The Biblical Biochemist-Where Science Meets the Cross"

God's Got You Covered

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