FDA MedWatch Alert Recall: Stud Capsule For Men
FDA MedWatch Alert Recall: Stud Capsule For Men
April 6, 2010
Audience: Consumers, Pharmacists.
April 6, 2010
Audience: Consumers, Pharmacists.
Kanec USA and FDA notified healthcare professionals of a nationwide
recall of Stud Capsule For Men [Lot #060607-01/060108-01, Exp 6-2013],
after being informed by FDA that laboratory analysis of a sample found
the product to be adulterated with sildenafil, an FDA approved drug.
Use of this product may pose a threat to consumers because the
analogue may interact with nitrates found in some prescription drugs
(such as nitroglycerin) and may lower blood pressure...
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