Nephron Sc Inc: Drug Recall
Recall #D-0178-2023 · 01/12/2023
Class II: Risk
Recall Details
- Recall Number
- D-0178-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Nephron Sc Inc
- Status
- Terminated
- Date Initiated
- 01/12/2023
- Location
- West Columbia, SC, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 389,730 vials
Reason for Recall
CGMP Deviations: potential for trace amounts of product carryover.
Product Description
Sterile Water for Injection, USP, For Drug Diluent Use Only, 5 mL Single-Dose Vial, packaged in 30 x 5 mL Single-Dose Vials per carton, Rx Only, Nephron Pharmaceuticals Corporation, 4500 12th Street Extension, W. Columbia, SC 29172, NDC 0487-6105-01, UPC 3 04876 10501 3.
Distribution Pattern
Nationwide in the USA
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 08/10/2022
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.