Vecuronium Bromide for Injection recall (Meitheal Pharmaceuticals, Inc)
DrugClass IIIOngoing
Summary: Meitheal Pharmaceuticals, Inc is recalling 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.
What is being recalled
Vecuronium Bromide for Injection, 10mg, 10 Single-Dose Vials per carton, Sterile, Rx Only, Mfd. for Meitheal Pharmaceuticals, Chicago, IL. NDC: 71288-744-11
Why
Labeling: Label Lacks Warning or Rx Legend
How serious is it
Class III is the least serious level: using or being exposed to this product is not likely to cause health problems, but it breaks FDA rules.
Where it was sold
US. Nationwide
How to tell if yours is affected
Lot# T1P0213A: Exp. 30-Apr-29 Lot# T1P0313A: Exp. 30-Apr-29 Lot# T1P0412A: Exp. 30-Sep-28 Lot# T1P0413A: Exp. 30-Apr-29 Lot# T1P0512A: Exp. 30-Sep-28 Lot# T1P0513A: Exp. 30-Apr-29
What to do
Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.
Recall facts
| Recall number | D-0108-2027 |
| Category | Drug |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class III |
| Status | Ongoing |
| Recall started | October 8, 2026 |
| Reported | November 4, 2026 |
| Company | Meitheal Pharmaceuticals, Inc |
| Company location | Chicago, IL, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 121,800 vials |
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