FDA·Healthcare and labs·December 10, 2025

Safecor Health recalls Haloperidol Lactate Injection vials over wrong RFID tag labels

The repackaging firm attached KITCHECK RFID tags with incorrect serial numbers to 800 one-milliliter vials of haloperidol injection, which could cause tracking mix-ups.

What to do

The notice does not give instructions. Read the official notice for details.

Recall details

Product
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.
Hazard
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
Units
800 1mL vials
Where sold
Distributed in Massachusetts
FDA classification
Class II · Ongoing
Classified by FDA
December 2, 2025
Recall started
October 10, 2025
FDA enforcement report
December 10, 2025
Identifiers
  • Codes: Lot 25381993 and 25391516, Exp 12/31/2026
  • FDA recall number: D-0214-2026

The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.

Official notice

The notice's own wording from FDA.

Product
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.
Classification
Class II (Ongoing)
Distribution
Distributed in Massachusetts
Quantity
800 1mL vials

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