CLASS II Drug recall · Reported 22 May 2019 · FDA Enforcement Report

CVS Health Children's Allergy Relief Liquid Medication recalled

Unipharma is recalling CVS Health Children's Allergy Relief Liquid Medication Diphenhydramine HCl 5 mg/ Oral, distributed nationwide in the US. The recall was initiated on 2 May 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots: 80058; 80059 Exp. 11/30/20
Quantity recalled27840 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-1300-2019
FDA event ID
82754
Recalling firm
Unipharma, Tamarac, FL
Classification
Class II
Status
Terminated
Recall initiated
2 May 2019
FDA classified
23 May 2019
Reported
22 May 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

2 May 2019Recall initiated by company
22 May 2019Published in enforcement report+20 days
23 May 2019Classified by FDA+1 day

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

Reason for recall

CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.

Product as listed by the FDA

CVS Health Children's Allergy Relief Liquid Medication Diphenhydramine HCl 12.5 mg/5 mL Oral Solution Antihistamine Mixed Berry Flavor 20 Single-Use 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC 69842-261-01, UPC 050428597156

Where it was distributed

Nationwide and Venezuela

Nationwide

Stores named: CVS

Questions about this recall

Is CVS Health Children's Allergy Relief Liquid Medication Diphenhydramine HCl 5 mg/ Oral recalled?

Yes. Unipharma recalled CVS Health Children's Allergy Relief Liquid Medication Diphenhydramine HCl 5 mg/ Oral on 2 May 2019. The recall is Class II and its status is Terminated. Recall number D-1300-2019.

Why was it recalled?

CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.

Which lots are affected?

Lots: 80058; 80059 Exp. 11/30/20

Where was it sold?

Nationwide and Venezuela

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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