CLASS I Drug recall · Reported 8 Feb 2023 · FDA Enforcement Report

CVS First Aid Home, First Aid Kit recalled by GFA Production Xiamen Co

GFA Production Xiamen Co is recalling CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream, distributed nationwide in the US. The recall was initiated on 23 Dec 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # W06H15, exp 08/15/2024
Quantity recalled15000 packets

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-0252-2023
FDA event ID
91410
Recalling firm
GFA Production Xiamen Co, Xiamen, N/A
Classification
Class I
Status
Terminated
Recall initiated
23 Dec 2022
FDA classified
27 Jan 2023
Reported
8 Feb 2023
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Sterility

Timeline

23 Dec 2022Recall initiated by company
27 Jan 2023Classified by FDA+35 days
8 Feb 2023Published in enforcement report+12 days

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

Reason for recall

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 2980-0700

Where it was distributed

Nationwide and Canada.

Nationwide

Stores named: CVS

Questions about this recall

Is CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream recalled?

Yes. GFA Production Xiamen Co recalled CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream on 23 Dec 2022. The recall is Class I and its status is Terminated. Recall number D-0252-2023.

Why was it recalled?

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Which lots are affected?

Lot # W06H15, exp 08/15/2024

Where was it sold?

Nationwide and Canada.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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