CLASS II Drug recall · Reported 12 Jan 2022 · FDA Enforcement Report

H.E.B Allergy Relief, Fexofenadine Hydrochloride tablets recalled

Perrigo Company is recalling H.E.B Allergy Relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/Antihistamine, distributed nationwide in the US. The recall was initiated on 27 Jul 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot a) 0HE2530, Exp 12/31/2021; 0JE2407, Exp 2/28/2022: b) 1BR0462, Exp 10/31/2022 c) 0FR0460, Exp 2/28/2022: 0LR0363, Exp 6/30/2022
Quantity recalled13,920 containers

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-0340-2022
FDA event ID
88384
Recalling firm
Perrigo Company, Allegan, MI
Classification
Class II
Status
Terminated
Recall initiated
27 Jul 2021
FDA classified
5 Jan 2022
Reported
12 Jan 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

27 Jul 2021Recall initiated by company
5 Jan 2022Classified by FDA+162 days
12 Jan 2022Published in enforcement report+7 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; Out of specification result obtained for impurity A during stability testing.

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

H.E.B Allergy Relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/Antihistamine packaged as a) 15 count bottle, NDC 37808-571-22, UPC 0 41220 53081 6; b) 30 count bottle, NDC 37808-571-39, UPC 0 41220 53082 3; c) 45 count bottle, NDC 37808-571-95, UPC 0 41220 53083 0; Made with Pride & Care for H.E.B. San Antonio TX 78204, Product of Czech Republic,

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Is H.E.B Allergy Relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/Antihistamine recalled?

Yes. Perrigo Company recalled H.E.B Allergy Relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/Antihistamine on 27 Jul 2021. The recall is Class II and its status is Terminated. Recall number D-0340-2022.

Why was it recalled?

Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.

Which lots are affected?

Lot a) 0HE2530, Exp 12/31/2021; 0JE2407, Exp 2/28/2022: b) 1BR0462, Exp 10/31/2022 c) 0FR0460, Exp 2/28/2022: 0LR0363, Exp 6/30/2022

Where was it sold?

Nationwide in 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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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