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
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-0903-2023
- FDA event ID
- 91672
- Recalling firm
- L. Perrigo, Allegan, MI
- 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
- Drug class
- Allergy Medication
Timeline
| 9 Feb 2023 | Recall initiated by company | |
| 11 Jul 2023 | Classified by FDA | +152 days |
| 19 Jul 2023 | Published 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, 30-count cartons, Distributed By: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 69842-0914-39
Where it was distributed
Nationwide within the USA
Stores named: CVS
Questions about this recall
Is Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg recalled?
Yes. L. Perrigo recalled Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg on 9 Feb 2023. The recall is Class II and its status is Terminated. Recall number D-0903-2023.
Why was it recalled?
Failed Impurities/Degradation Specifications
Which lots are affected?
Lot #: 2DV1925, Exp. date 06/23
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 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.
More recalls from L. Perrigo
All 28| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | aller-ease, Fexofenadine Hydrochloride Tablets, 180 mg recalledExchange Select Aller Ease | L. Perrigo | Potency & Assay | Nationwide |
| Drug | CLASS II | Allergy Aller-fex, Fexofenadine Hydrochloride Tablets, 180 mg recalledKirkland Signature Aller Fex | L. Perrigo | Potency & Assay | Nationwide |
| Drug | CLASS II | Non-Drowsy Allergy Relief, Fexofenadine Hydrochloride recalledBerkley Jensen Allergy Relief | L. Perrigo | Potency & Assay | Nationwide |
| Drug | CLASS II | Allergy, Fexofenadine Hydrochloride Tablets, 180 mg recalledBasic Care Allergy | L. Perrigo | Potency & Assay | Nationwide |
| Drug | CLASS II | Picnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine recalled | L. Perrigo | Potency & Assay | Nationwide |