Nephron Sc Inc: Drug Recall
Recall #D-1354-2022 · 08/10/2022
Class II: Risk
Recall Details
- Recall Number
- D-1354-2022
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Nephron Sc Inc
- Status
- Terminated
- Date Initiated
- 08/10/2022
- Location
- West Columbia, SC, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5040 vials
Reason for Recall
cGMP Deviations: deviations leading to potential cross-contamination.
Product Description
Ketorolac Tromethamine Injection, USP 60 mg/2 mL (30 mg/mL), packaged in 2 mL single dose vials, Rx Only, Nephron Pharmaceutical Corporation 4500 12th Street Extension West Columbia, SV 29172, NDC 0487-6232-01
Distribution Pattern
USA Nationwide
Other Recalls by Nephron Sc Inc
- Class II: Risk 02/23/2023
- Class II: Risk 01/13/2023
- Class II: Risk 01/13/2023
- Class II: Risk 01/12/2023
- Class II: Risk 01/12/2023
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.