Meitheal Pharmaceuticals, Inc: Vecuronium Bromide For Injection, 10mg, 10 Single-dose Vials Per Carton, Sterile
Recall Summary Meitheal Pharmaceuticals is recalling Vecuronium Bromide for Injection (10mg vials) distributed nationwide because the product labeling is missing required warnings and the prescription-only legend. Vecuronium Bromide is a prescription medication used during surgery and medical procedures. This is a Class III recall, the least serious classification.
- Recalling firm
- Meitheal Pharmaceuticals, Inc
- Product
- Vecuronium Bromide for Injection, 10mg, 10 Single-Dose Vials per carton, Sterile, Rx Only, Mfd. for Meitheal Pharmaceuticals, Chicago, IL. NDC: 71288-744-11
- Reason
- Labeling: Label Lacks Warning or Rx Legend
- Classification
- Class III
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-10-08
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US. Nationwide
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/29d29128-8287-46a5-a957-3c9c100da560