D-0109-2027 Class III Ongoing
FDA drug recall D-0109-2027 was initiated by Meitheal Pharmaceuticals, Inc on Oct 8, 2026 and is designated Class III. Reason for recall: Labeling: Label Lacks Warning or Rx Legend The recall status is ongoing. Affected quantity: 10,200 vials.
Recall Details
- Product Type
- Drugs
- Report Date
- Nov 4, 2026
- Initiation Date
- Oct 8, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10,200 vials
Product Description
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 for Recall
Labeling: Label Lacks Warning or Rx Legend
Distribution Pattern
US. Nationwide
Code Information
Lot# T1P0113C: Exp. 28-Feb-29 Lot# T1P0612C: Exp. 31-Oct-28
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0109-2027
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026