Teva Pharmaceuticals USA recalls Niacin Extended Release Tablets, USP, 500 mg, 90 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., Sellersville, PA
Recalled January 8, 2014 · FDA recall D-396-2014 · Teva Pharmaceuticals USA
Hazard
Failed Tablet/Capsule Specifications: There is a potential for broken tablets. · FDA Class II
Units
10,512 bottles
Sold at
Nationwide and Puerto Rico, American Samoa, Virgin Islands, and Canal Zone
Description
Failed Tablet/Capsule Specifications: There is a potential for broken tablets.
Product
Niacin Extended Release Tablets, USP, 500 mg, 90 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., Sellersville, PA, 18960, NDC 0093-7392-98
Manufacturer(s)
Teva Pharmaceuticals USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →