Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 180 mg, 30-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314, USA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, USA; NDC 52544-691-30.
Reported: August 10, 2022 Initiated: July 21, 2022 #D-1302-2022
Product Description
Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 180 mg, 30-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314, USA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, USA; NDC 52544-691-30.
Reason for Recall
Failed Dissolution Specifications: below specification limits for dissolution.
Details
- Recalling Firm
- Teva Pharmaceuticals USA Inc
- Units Affected
- 8022 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, 180 mg, 30-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314, USA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, USA; NDC 52544-691-30.. Recalled by Teva Pharmaceuticals USA Inc. Units affected: 8022 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-1302-2022.
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