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
Reported: October 16, 2019 Initiated: September 6, 2019 #D-0131-2020
Product Description
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
Reason for Recall
GMP Deviation: lot not intended for commercial distribution.
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 5,849 bottles
- Distribution
- 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.
- Location
- Parsippany, NJ
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Teva Pharmaceuticals USA. Units affected: 5,849 bottles.
Why was this product recalled? ▼
GMP Deviation: lot not intended for commercial distribution.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 16, 2019. Severity: Low. Recall number: D-0131-2020.
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