Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by Teva Pharmaceuticals USA Inc Due to Failed Dissolution Specifications: below specification limits for dissolution.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teva Pharmaceuticals USA Inc directly.
Affected Products
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.
Quantity: 5677 bottles
Why Was This Recalled?
Failed Dissolution Specifications: below specification limits for dissolution.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA Inc
Teva Pharmaceuticals USA Inc has 20 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report