Safecor Health, LLC recalls Haloperidol Lactate Injection
- Recalling company
- Safecor Health, LLC
- 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
- Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Oct 10, 2025
- Reported
- Dec 10, 2025
- Distribution
- Distributed in Massachusetts
- Status
- Ongoing
- Quantity
- 800 1mL vials
- Lot / codes
- Lot 25381993 and 25391516, Exp 12/31/2026
- Company location
- Woburn, MA
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0214-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0214-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.