Somerset Therapeutics Private Limited: Drug Recall
Recall #D-0356-2025 · 03/21/2025
Class II: Risk
Recall Details
- Recall Number
- D-0356-2025
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Somerset Therapeutics Private Limited
- Status
- Ongoing
- Date Initiated
- 03/21/2025
- Location
- Bengaluru, N/A, India
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4956 vials
Reason for Recall
Lack of Assurance of Sterility: Media fill with bacterial contamination
Product Description
Haloperidol Decanoate Injection 50mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by: Somerset Therapeutics Limited, Kamataka India, Manufactured for: BluePoint Laboratories NDC 68001-580-41
Distribution Pattern
U.S. Nationwide
Other Recalls by Somerset Therapeutics Private Limited
- Class II: Risk 03/21/2025
- Class II: Risk 03/21/2025
- Class II: Risk 03/21/2025
- Class II: Risk 03/21/2025
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.