D-0019-2025 Class II Terminated
FDA drug recall D-0019-2025 was initiated by Fresenius Kabi Compounding, LLC on September 25, 2024 and is designated Class II. Reason for recall: cGMP violations The recall status is terminated (terminated August 15, 2025). Affected quantity: 2151 bags.
Recall Details
- Product Type
- Drugs
- Report Date
- October 30, 2024
- Initiation Date
- September 25, 2024
- Termination Date
- August 15, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2151 bags
Product Description
NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP, 4 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-025-58
Reason for Recall
cGMP violations
Distribution Pattern
Product was distributed to 125 direct accounts nationwide.
Code Information
Lot # C274-000038582, exp. date 29-Nov-24