Teva Pharmaceuticals USA recalls Metformin Hydrochloride Extended Release Tablets 1000 mg, 90-count bottle, Rx only, Manufactured by: Actavis Laboratorie

Recalled October 31, 2018 · FDA recall D-0101-2019 · Teva Pharmaceuticals USA

Hazard

Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release. · FDA Class II

Units

N/A

Sold at

Product was distributed throughout the United States. Bulk product was distributed to Takeda, Deerfield, IL and may have been further distributed.

Description

Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.

Product

Metformin Hydrochloride Extended Release Tablets 1000 mg, 90-count bottle, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL, 33314, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 , NDC 00591-2412-19

Manufacturer(s)

Teva Pharmaceuticals USA

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →