Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30-count bottles, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL USA 33314, USA, Distributed by: Actavis Pharma Inc., Parsippany, NJ 07054 USA; NDC 58544-692-30.
Reported: August 10, 2022 Initiated: July 21, 2022 #D-1303-2022
Product Description
Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30-count bottles, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL USA 33314, USA, Distributed by: Actavis Pharma Inc., Parsippany, NJ 07054 USA; NDC 58544-692-30.
Reason for Recall
Failed Dissolution Specifications: below specification limits for dissolution.
Details
- Recalling Firm
- Teva Pharmaceuticals USA Inc
- Units Affected
- 5677 bottles
- Distribution
- Nationwide in the USA and Puerto Rico
- Location
- Parsippany, NJ
Frequently Asked Questions
What product was recalled? ▼
Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30-count bottles, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL USA 33314, USA, Distributed by: Actavis Pharma Inc., Parsippany, NJ 07054 USA; NDC 58544-692-30.. Recalled by Teva Pharmaceuticals USA Inc. Units affected: 5677 bottles.
Why was this product recalled? ▼
Failed Dissolution Specifications: below specification limits for dissolution.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 10, 2022. Severity: Moderate. Recall number: D-1303-2022.
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