VECURONIUM BROMIDE
Recalling Firm / Manufacturer: Meitheal Pharmaceuticals, Inc
(Chicago, IL, United States)
FDA Recall Number: D-0109-2027
Source Authority Disclaimer: This drug recall notice is published by Questo using official enforcement reports issued by the U.S. Food & Drug Administration (FDA). It is provided for informational, academic, and clinical research purposes only. Patients should not discontinue prescribed treatments without consulting their physician or pharmacist.
Product & Identification Information
Brand, active ingredients, NDC codes, and manufacturer details
Brand / Trade Name
VECURONIUM BROMIDE
Generic Name
VECURONIUM BROMIDE
Active Substance(s)
Vecuronium Bromide
Administration Route
Intravenous
National Drug Code (NDC)
71288-744
Total Quantity Recalled
10,200 vials
Official Reason for Recall
Specific hazard or quality defect cited by the FDA
According to the official FDA enforcement report:
Labeling: Label Lacks Warning or Rx Legend
Full Product Description
Packaging specifications and labeling details
Vecuronium Bromide for Injection, 20mg, 10 Single-Dose Vials per carton, Sterile, Rx Only, Mfd. for Meitheal Pharmaceuticals, Chicago, IL. NDC: 71288-745-21
Enforcement & Regulatory Details
FDA classification, report dates, and initiation authority
Health Hazard Classification
Class III
Current Action Status
Ongoing
FDA Enforcement Report Date
November 04, 2026
Firm Initiation Date
October 08, 2026
FDA Classification Date
Oct 29, 2026
Initiation Type
Voluntary: Firm initiated
Affected Lots & Batch Numbers
Product codes, lot numbers, and expiration dates
Lot# T1P0113C: Exp. 28-Feb-29 Lot# T1P0612C: Exp. 31-Oct-28
Distribution Information
Geographic scope of affected shipments
US. Nationwide
Safety Guidance & Actions
Standard FDA protocol for patients and healthcare providers
Advisory Notice
This Class III recall involves technical or packaging non-conformities that are not expected to cause adverse health consequences. Consult your pharmacist if you have questions.
Official Source Provenance
Verified regulatory citation from U.S. FDA OpenFDA
Primary Data Source: U.S. Food & Drug Administration (FDA) OpenFDA API
Recall Number: D-0109-2027
Questo Retrieval Date: November 10, 2026 12:00 1794312006UTCC