FDA Announces 'Stud Capsule' Recall

WASHINGTON, April 8 (UPI) — The U.S. Food and Drug Administration announced the nationwide recall of an erectile dysfunction product called “Stud Capsule for Men.”

The FDA said the product, distributed by Kanec USA Inc. of Davie, Fla., contains sildenafil, a drug that can pose a health hazard because it might interact with nitrates found in some prescription medications and might lower blood pressure to a dangerous level.


Being recalled is Lot. No. 060607-01/060108-01 with an expiration date of “6-2013.” Stud Capsule for Men is sold in a blister pack containing one capsule per unit with 24-packs in a box. The lot number and expiration date appear on the seal.

The product can be returned for a refund. Customers with questions can contact the company at 954-583-5840.

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