Warning
Safecor Health Recalls Haloperidol Lactate Injection
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0214-2026Drug / Pharmaceutical
Safecor Health Recalls Haloperidol Lactate Injection
Safecor Health, LLC · Class II — Moderate Risk
Product Description
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.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Distributed in Massachusetts
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA classified this recall as Class II, indicating the pharmaceutical product may cause temporary health problems or poses a slight threat of a serious nature. Safecor Health, LLC initiated the recall on October 10, 2025 affecting 800 1mL vials. Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm. The product was distributed in Distributed in Massachusetts. Consumers should check their purchases and discontinue use of any affected product. Contact Safecor Health, LLC for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.