CLASS II Drug recall · Reported 19 Jul 2023 · FDA Enforcement Report

allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg recalled

L. Perrigo is recalling allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, distributed nationwide in the US. The recall was initiated on 9 Feb 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: a) 2JE1882, Exp. date 01/24 b) 2FV1918, 2ER0411, Exp. date 01/24; 2GV1902, Exp. date 04/24; 2CR0652, 2DR0465, Exp. date 12/23; 2GR0329, Exp. date 04/24 c)2CR0653, 2DR0466, Exp. date 12/23; 2ER0287, 2ER0412, Exp. date 01/24
NDC79481-0847
Quantity recalled59,688 cartons

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0906-2023
FDA event ID
91672
Recalling firm
L. Perrigo, Allegan, MI
Manufacturer
Meijer, Inc.
Classification
Class II
Status
Terminated
Recall initiated
9 Feb 2023
FDA classified
11 Jul 2023
Reported
19 Jul 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

9 Feb 2023Recall initiated by company
11 Jul 2023Classified by FDA+152 days
19 Jul 2023Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Failed Impurities/Degradation Specifications

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

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.

Where it was distributed

Nationwide within the USA

Nationwide

Stores named: Meijer

Questions about this recall

Why was it recalled?

Failed Impurities/Degradation Specifications

Which lots are affected?

Lot #: a) 2JE1882, Exp. date 01/24 b) 2FV1918, 2ER0411, Exp. date 01/24; 2GV1902, Exp. date 04/24; 2CR0652, 2DR0465, Exp. date 12/23; 2GR0329, Exp. date 04/24 c)2CR0653, 2DR0466, Exp. date 12/23; 2ER0287, 2ER0412, Exp. date 01/24

Where was it sold?

Nationwide within the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

12 other products · FDA event 91672

This product is part of a recall event; the main page for the event is allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIallergy relief, Fexofenadine Hydrochloride Tablets, 180 mg recalledL. PerrigoPotency & AssayNationwide
CLASS IIAllergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg recalledTopcare Allergy ReliefL. PerrigoPotency & AssayNationwide
CLASS IIallergyrelief, Fexofenadine Hydrochloride Tablets, 180 mg recalledAllergy ReliefL. PerrigoPotency & AssayNationwide
CLASS IIAllergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg recalledL. PerrigoPotency & AssayNationwide
CLASS IIFexofenadine Hydrochloride Tablets, 180 mg recalled by L. PerrigoFexofenadine HydrochlorideL. PerrigoPotency & AssayNationwide
CLASS IIAllergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg recalledCareone Allergy ReliefL. PerrigoPotency & AssayNationwide
CLASS IIFexofenadine Hydrochloride Tablets, 180 mg recalled by L. PerrigoGood Sense Aller EaseL. PerrigoPotency & AssayNationwide
CLASS IIPicnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine recalledL. PerrigoPotency & AssayNationwide
CLASS IIAllergy, Fexofenadine Hydrochloride Tablets, 180 mg recalledBasic Care AllergyL. PerrigoPotency & AssayNationwide
CLASS IINon-Drowsy Allergy Relief, Fexofenadine Hydrochloride recalledBerkley Jensen Allergy ReliefL. PerrigoPotency & AssayNationwide
CLASS IIAllergy Aller-fex, Fexofenadine Hydrochloride Tablets, 180 mg recalledKirkland Signature Aller FexL. PerrigoPotency & AssayNationwide
CLASS IIaller-ease, Fexofenadine Hydrochloride Tablets, 180 mg recalledExchange Select Aller EaseL. PerrigoPotency & AssayNationwide

More recalls from L. Perrigo

All 28
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIaller-ease, Fexofenadine Hydrochloride Tablets, 180 mg recalledExchange Select Aller EaseL. PerrigoPotency & AssayNationwide
DrugCLASS IIAllergy Aller-fex, Fexofenadine Hydrochloride Tablets, 180 mg recalledKirkland Signature Aller FexL. PerrigoPotency & AssayNationwide
DrugCLASS IINon-Drowsy Allergy Relief, Fexofenadine Hydrochloride recalledBerkley Jensen Allergy ReliefL. PerrigoPotency & AssayNationwide
DrugCLASS IIAllergy, Fexofenadine Hydrochloride Tablets, 180 mg recalledBasic Care AllergyL. PerrigoPotency & AssayNationwide
DrugCLASS IIPicnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine recalledL. PerrigoPotency & AssayNationwide

Other Fexofenadine recalls

All 32