Lundbeck LLC: Drug Recall
Recall #D-1142-2023 · 08/17/2023
Class III: Low Risk
Recall Details
- Recall Number
- D-1142-2023
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Lundbeck LLC
- Status
- Completed
- Date Initiated
- 08/17/2023
- Location
- Deerfield, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10,543 cartons
Reason for Recall
Cross contamination with other products
Product Description
Sabril (vigabatrin) for Oral Solution, 500 mg, 50 Packets, Rx only, Manufactured by: Patheon, Cincinnati, OH 45237, NDC 67386-211-65
Distribution Pattern
Nationwide within the U.S.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.