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Teva Pharmaceuticals USA recalls Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30 count bottle, Rx only, Manufactured by: Actabis

Recalled October 16, 2019 · FDA recall D-0131-2020 · Teva Pharmaceuticals USA

Hazard
GMP Deviation: lot not intended for commercial distribution. · FDA Class III
Units
5,849 bottles
Sold at
Product was distributed to 42 wholesalers and 11 retailers who may have further distribute the product throughout the United States, including Hawaii and Puerto Rico.

Description

GMP Deviation: lot not intended for commercial distribution.

Product
Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30 count bottle, Rx only, Manufactured by: Actabis Laboratories FL, Inc., Fort Lauderdale, FL, Distributed by: Actavis Pharma, Inc., Parsippany, NJ NDC 52544-692-30
Manufacturer(s)
Teva Pharmaceuticals USA

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

Teva Pharmaceuticals USA recalls Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30 count bottle, Rx only, Manufactured by: Actabis | RecallWatchUSA