Meitheal Pharmaceuticals, Inc: Vecuronium Bromide For Injection, 20mg, 10 Single-dose Vials Per Carton, Sterile
Recall Summary Meitheal Pharmaceuticals is recalling Vecuronium Bromide for Injection (20mg vials) distributed nationwide because the product labeling is missing required warning information and the prescription-only legend. Vecuronium Bromide is a prescription medication used during anesthesia, and this recall affects all states in the US.
- Recalling firm
- Meitheal Pharmaceuticals, Inc
- Product
- Vecuronium Bromide for Injection, 20mg, 10 Single-Dose Vials per carton, Sterile, Rx Only, Mfd. for Meitheal Pharmaceuticals, Chicago, IL. NDC: 71288-745-21
- 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/05937b30-247b-453a-81a0-5f96c3f73a53