Haloperidol Lactate Injection — Class II drug recall D-0214-2026
Ongoing recall by Safecor Health, LLC, reported 2025-12-10, distributed in MA. Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
| Recall number | D-0214-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Safecor Health, LLC, Woburn, MA, United States |
| Recall initiated | 2025-10-10 |
| Classified | 2025-12-02 |
| Reported by FDA | 2025-12-10 |
| Distributed | MA |
| Quantity | 800 |
| Reason classes | labeling |
| NDC | 67457-0426, 67457-0426-00, 67457-0426-12 |
| Lot numbers | 25381993, 25391516 |
| Expiration dates | 2026-12-31 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0214-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.