L. Perrigo Company: Drug Recall
Recall #D-0906-2023 · 02/09/2023
Class II: Risk
Recall Details
- Recall Number
- D-0906-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- L. Perrigo Company
- Status
- Terminated
- Date Initiated
- 02/09/2023
- Location
- Allegan, MI, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 59,688 cartons
Reason for Recall
Failed Impurities/Degradation Specifications
Product Description
allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 79481-0847-0), b)30-count cartons (NDC 79481-0847-1), and c) 45-count cartons (NDC 79481-0847-2), Distributed by: MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544.
Distribution Pattern
Nationwide within the USA
Other Recalls by L. Perrigo Company
- Class II: Risk 02/09/2023
- Class II: Risk 02/09/2023
- Class II: Risk 02/09/2023
- Class II: Risk 02/09/2023
- Class II: Risk 02/09/2023
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.