Teva Pharmaceuticals Usa, Inc: Metoclopramide Tablets, Usp, 5 Mg, [100 Or 500] Tablets Per Bottle
Recall Summary Teva Pharmaceuticals is recalling Metoclopramide Tablets, USP 5 mg (in bottles of 100 or 500 tablets) distributed nationwide because some bottles contain foreign tablets or capsules mixed in with the medication. The affected NDC codes are 0093-2204-01 and 0093-2204-05. This recall applies to all U.S. states and territories.
- Recalling firm
- Teva Pharmaceuticals USA, Inc
- Product
- Metoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC 100 Tablets: 0093-2204-01; NDC 500 Tablets: 0093-2204-05
- Reason
- Presence of Foreign Tablets/Capsules
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-09-29
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/c5d410a9-d9b5-4032-a0be-68094653bac6