Teva Pharmaceuticals USA recalls Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc.
Recalled November 1, 2017 · FDA recall D-0052-2018 · Teva Pharmaceuticals USA
Hazard
Failed Dissolution Specifications: Low out of specification results for dissolution. · FDA Class III
Units
58,292 bottles
Sold at
Nationwide in the USA and Puerto Rico
Description
Failed Dissolution Specifications: Low out of specification results for dissolution.
Product
Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 0591-5884-01.
Manufacturer(s)
Teva Pharmaceuticals USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →