FDAFDA · Food and drugs·Recall number D-0023-2025
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
Published October 30, 2024 · Recall initiated: September 25, 2024
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
cGMP violations
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Fresenius Kabi Compounding, LLC
- Distributor
- Product was distributed to 125 direct accounts nationwide.
- Lot
- Lot # C274-000037436, exp. date 30-Oct-24 C274-000038893, exp. date 7-Jan-25
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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