FDAFDA · Food and drugs·Recall number 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.
Published December 10, 2025 · Recall initiated: October 10, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- HALOPERIDOL LACTATE
- Manufacturer
- Safecor Health, LLC
- Distributor
- Distributed in Massachusetts
- Lot
- Lot 25381993 and 25391516, Exp 12/31/2026
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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