# FDA recall D-1303-2022

> **Teva Pharmaceuticals USA Inc** · Class II · drug recall initiated 2022-07-21.

## Product

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.

## Distribution

Nationwide in the USA and Puerto Rico

## Key facts

- **Recall number:** D-1303-2022
- **Recalling firm:** Teva Pharmaceuticals USA Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-07-21
- **Report date:** 2022-08-10
- **Termination date:** 2023-04-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Parsippany, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1303-2022

## Citation

> AI Analytics. FDA recall D-1303-2022. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/D-1303-2022. Source: US FDA. Licensed CC0.

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