FDA Drugs recall ·
Vecuronium Bromide for Injection, 20mg, 10 Single-Dose Vials per carton… recall
- Recall number
- D-0109-2027
- Date
- (initiated October 8, 2026)
- Company / brand
- Meitheal Pharmaceuticals, Inc
8700 W Bryn Mawr Ave Ste 600s, Chicago, IL, United States - Category
- Drugs › Class III
- Classification
- Class III
- Status
- Ongoing
- Units affected
- 10,200 vials
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it recalled?
Labeling: Label Lacks Warning or Rx Legend
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot# T1P0113C: Exp. 28-Feb-29 Lot# T1P0612C: Exp. 31-Oct-28
Distribution
US. Nationwide
What does Class III mean?
Class III means use of or exposure to the product is not likely to cause adverse health consequences (for example, a labeling violation).
Source: FDA (drugs), recall D-0109-2027. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.