Astral SteriTech Private Ltd.: Drug Recall
Recall #D-0591-2023 · 05/15/2023
Class II: Risk
Recall Details
- Recall Number
- D-0591-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Astral SteriTech Private Ltd.
- Status
- Terminated
- Date Initiated
- 05/15/2023
- Location
- Vadodara, N/A, India
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 419,680 vials
Reason for Recall
Lack of Assurance of Sterility
Product Description
Ampicillin and Sulbactam for Injection, USP 3 gram per vial, Rx only, Manufactured for: Civica Inc. Lehi Utah 84043, NDC 72572-022-10
Distribution Pattern
Nationwide within the United States
Other Recalls by Astral SteriTech Private Ltd.
- Class II: Risk 05/15/2023
- Class II: Risk 05/15/2023
- Class II: Risk 05/15/2023
- Class II: Risk 05/15/2023
- Class II: Risk 05/15/2023
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.