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From Rev Barb: I am certain that Dear Ones Healing Ministry Readers are WAY too smart to use this stuff below
Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed As a Dietary Supplement
http://www.fda.gov/Safety/Recalls/ucm206759.htm
Contact Person:
Alex Treynker
(954) 570-6662
FOR IMMEDIATE RELEASE -- March 30, 2010 - Natural Wellness is warning consumers not to purchase or consume the product known as MasXtreme, Lot# 911035. This product which is being marketed as a dietary supplement contains undeclared amounts of Aildenafil, as well as the drug Phentolamine which is an alpha-adrenergic blocker. Aildenafil is close in structure to Sildenafil and is expected to possess a similar pharmacological and adverse event profile. Sildenafil is the active pharmaceutical ingredient in an FDA-approved drug that is used to treat erectile dysfunction (ED). This may pose a threat to consumers because Aildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Common side effects of Phentolamine include arrhythmia (abnormal heart rhythm) and tachycardia (rapid heart beat).
MasXtreme is sold in blister packs containing one (1) capsule. The product is distributed Nationwide by Natural Wellness Inc. This product is being promoted for increasing desire and sexual performance. The product is sold without medical prescription.
Consumers who have purchased MasXtreme tablets are urged to immediately discontinue their use and return the product to their place of purchase or directly to Natural Wellness Inc. at 440 S Federal Hwy, Suite 107, Deerfield Beach, FL 33441. Consumers with questions regarding this recall may contact the company at 954-570-6662 Monday through Friday 8 am to 4 pm. Consumers who have purchased this product and have medical concerns should consult with their health care providers.
Adverse reaction or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program online, by regular mail, or by fax. Online: www.fda.gov/MedWatch/report.htm1. Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at www.fda.gov/MedWatch/getforms.htm2. Mail to address on the pre-addressed form. Fax: 1-800-FDA-0178.
This recall is being conducted in cooperation with the U.S. Food and Drug Administration (FDA).
http://www.fda.gov/Safety/Recalls/ucm206759.htm
And For Michigan ONLY, PEPPER ALERT:Binell Bros. Cutlery Voluntarily Recalls Black Pepper
http://www.fda.gov/Safety/Recalls/ucm206806.htm
Company Contact:
Robert G. Ramsay ,
313-584-3219
FOR IMMEDIATE RELEASE - March 30, 2010 - As the result of a recall of Black Pepper by Mincing Overseas Spice Company, Binell Bros. of Dearborn, MI is recalling ground black pepper because it has the potential to be contaminated with Salmonella. The pepper is packaged in clear, plastic bags weighing between ¼ lb and 10 lbs, and was sold on-site between December 11, 2009 and February 2, 2010. The bags are labeled with stickers identifying the distributor, Binell Bros. Cutlery, but no product code. The product was sold in Michigan only.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
To date, no illnesses have been reported to Binell Bros. Cutlery. However, due to its commitment to the
health and safety of consumers, the company has decided to voluntarily initiate this recall.
Customers who have purchased any size quantities of ground black pepper between the dates of December 11, 2009 and February 2, 2010 should stop using the pepper, and return it to Binell Bros. Cutlery for full refund. For more information, customers may call 313-584-3219 from 9-4 EST Monday - Friday.
http://www.fda.gov/Safety/Recalls/ucm206806.htm
Please Be Careful & Stay Well!
Rev Barb Sexton
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