Performance Plus Marketing, Inc. recalls BLUE Diamond PLATINUM Capsules, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed By: DH Distribution Lo
Recalled May 22, 2013 · FDA recall D-335-2013 · Performance Plus Marketing
Hazard
Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs · FDA Class I
Units
1,000 capsules.
Sold at
Nationwide
Description
Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs
Product
BLUE Diamond PLATINUM Capsules, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed By: DH Distribution Los Angeles, CA 90026 1 count blister UPC -608641933543; 5 count blister UPC - 608641932867; 10 count UPC -608641933536
Manufacturer(s)
Performance Plus Marketing, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →