United StatesHaloperidol Lactate Injection 5 mg/mL, 25 x 1 mL single‑dose vials (NDC 67457-426-12), lots 25381993 and 25391516, exp 12/31/2026, manufactured for Mylan Institutional and distributed in Massachusetts, is affected. Safecor Health is recalling 800 vials because KITCHECK RFID tags with incorrect serial numbers (KITCHECK 8001-03A3,00000000,003A-2560 and 8001-03A3,00000000,003A-2D3B) were applied to the product.
What's being 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.
Recalling firm: Safecor Health, LLC, Woburn, MA, United States.
How to identify it
Lot 25381993 and 25391516, Exp 12/31/2026
The hazard
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Distributed in Massachusetts
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)