Fresenius Kabi Compounding, LLC recalls Thiamine HCl 0.9% Sodium Chloride Injection USP, 500 mg per 100 mL, Single Dose Bag, Rx only, Fagron Sterile Services, C
Recalled October 30, 2024 · FDA recall D-0023-2025 · Fresenius Kabi Compounding
Hazard
cGMP violations · FDA Class II
Units
1008 bags
Sold at
Product was distributed to 125 direct accounts nationwide.
Description
cGMP violations
Product
Thiamine HCl 0.9% Sodium Chloride Injection USP, 500 mg per 100 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-079-56
Manufacturer(s)
Fresenius Kabi Compounding, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →