PlainRecalls
FDA Drug Moderate Class II Ongoing

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.

Reported: December 10, 2025 Initiated: October 10, 2025 #D-0214-2026

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.

Reason for Recall

Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.

Details

Recalling Firm
Safecor Health, LLC
Units Affected
800 1mL vials
Distribution
Distributed in Massachusetts
Location
Woburn, MA

Frequently Asked Questions

What product was recalled?
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.. Recalled by Safecor Health, LLC. Units affected: 800 1mL vials.
Why was this product recalled?
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 10, 2025. Severity: Moderate. Recall number: D-0214-2026.