Class II
Ongoing
Budesonide Extended-Release Tablets 9mg, 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 0591-2510-30
This recall is currently active, issued February 7, 2024. It was issued by Teva Pharmaceuticals Usa, Inc.
- Company
- Teva Pharmaceuticals Usa, Inc
- Recall Initiated
- January 8, 2024
- Posted
- February 7, 2024
- Recall Number
- D-0275-2024
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 10,672 30-count bottles
- Firm Location
- Parsippany, NJ, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Dissolution Specifications
Distribution
Nationwide
Lot / Code Info
Lot # 100047273; Exp. 07/2025
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