L. Perrigo Company: Drug Recall

Recall #D-0912-2023 · 02/09/2023

Class II: Risk

Recall Details

Recall Number
D-0912-2023
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
44,280 cartons

Reason for Recall

Failed Impurities/Degradation Specifications

Product Description

Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 36800-691-39), b)45-count cartons (NDC 36800-691-95), and 90-count cartons (NDC 36800-691-75), Distributed by: Topco Associates LLC, Elk Grove Village, IL 60007.

Distribution Pattern

Nationwide within the USA

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.