Home / Recalls / L. Perrigo Company / D-0907-2023

D-0907-2023 Class II Terminated

Recalled by L. Perrigo Company — Allegan, MI

FDA drug recall D-0907-2023 was initiated by L. Perrigo Company on Feb 9, 2023 and is designated Class II. Reason for recall: Failed Impurities/Degradation Specifications The recall status is terminated (terminated Sep 11, 2023). Affected quantity: 15,504 cartons.

Recall Details

Product Type: Drugs
Report Date: Jul 19, 2023
Initiation Date: Feb 9, 2023
Termination Date: Sep 11, 2023
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 15,504 cartons

Product Description

Fexofenadine Hydrochloride Tablets, 180 mg, 100-count cartons, Distributed by: Perrigo, Allegan, MI 49010. NDC 45802-847-78

Reason for Recall

Failed Impurities/Degradation Specifications

Distribution Pattern

Nationwide within the USA

Code Information

Lot #: 2DR0351, Exp. date 12/23

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0907-2023
openFDA file date: Nov 3, 2026
Loaded by RegDataLab: Nov 4, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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