Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Haloperidol Lactate Injection Recalled by Safecor Health, LLC Due to Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied...

Date: October 10, 2025
Company: Safecor Health, LLC
Status: Ongoing
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Safecor Health, LLC directly.

Affected Products

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.

Quantity: 800 1mL vials

Why Was This Recalled?

Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.

Where Was This Sold?

Distributed in Massachusetts

About Safecor Health, LLC

Safecor Health, LLC has 22 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report