Recalls / Class II
Class IID-0023-2025
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
- Affected lot / code info
- Lot # C274-000037436, exp. date 30-Oct-24 C274-000038893, exp. date 7-Jan-25
Why it was recalled
cGMP violations
Recalling firm
- Firm
- Fresenius Kabi Compounding, LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 20 Dan Rd, N/A, Canton, Massachusetts 02021-2809
Distribution
- Quantity
- 1008 bags
- Distribution pattern
- Product was distributed to 125 direct accounts nationwide.
Timeline
- Recall initiated
- 2024-09-25
- FDA classified
- 2024-10-21
- Posted by FDA
- 2024-10-30
- Terminated
- 2025-08-15
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0023-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.