FDA Drug · D-0214-2026

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.

Class II · Ongoing

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

Affected lots / codes — check yours against thisLot 25381993 and 25391516, Exp 12/31/2026

Recalling firm: Safecor Health, LLC, Woburn, MA
Classification: Class II (temporary or reversible harm possible)
Status: Ongoing
Quantity: 800 1mL vials
Distribution: Distributed in Massachusetts
Recall initiated: October 10, 2025
Classified: December 2, 2025
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0214-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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