ALEMBIC PHARMACEUTICALS, INC.: Drug Recall
Recall #D-0941-2023 · 06/22/2023
Class II: Risk
Recall Details
- Recall Number
- D-0941-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- ALEMBIC PHARMACEUTICALS, INC.
- Status
- Ongoing
- Date Initiated
- 06/22/2023
- Location
- Bedminster, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2844 units
Reason for Recall
Defective Delivery System
Product Description
Diclofenac Sodium Topical Solution USP, 2% w/w, 3.8 FL.OZ.(112 grams) bottles, Rx only, Manufactured for: Alembic Pharmaceuticals, Inc. Bedminster, NJ 07921, USA Manufactured by: Alembic Pharmaceuticals Limited (Derma Division) Karakhadi, Vadodara 391450, India. NDC 62332-487-12
Distribution Pattern
Nationwide within the United States
Other Recalls by ALEMBIC PHARMACEUTICALS, INC.
- Class III: Low Risk 07/27/2023
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.