Safecor Health, LLC: Drug Recall
Recall #D-0214-2026 · 10/10/2025
Class II: Risk
Recall Details
- Recall Number
- D-0214-2026
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Safecor Health, LLC
- Status
- Ongoing
- Date Initiated
- 10/10/2025
- Location
- Woburn, MA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 800 1mL vials
Reason for Recall
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
Product Description
Haloperidol Lactate Injection, 5 mg/mL, 25 x 1 mL Single-Dose Vials, Sterile, Rx only, For Intramuscular Use Only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26605. NDC: 67457-426-12 with Safecor Health LLC KITCHECK RFID Tag attached with incorrect serial numbers: KITCHECK 8001-03A3,00000000,003A-2560, and 8001-03A3,00000000,003A-2D3B.
Distribution Pattern
Distributed in Massachusetts
Other Recalls by Safecor Health, LLC
- Class II: Risk 02/17/2025
- Class II: Risk 02/17/2025
- Class II: Risk 02/17/2025
- Class II: Risk 02/17/2025
- Class II: Risk 02/17/2025
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.