CLASS I Drug recall · Reported 8 Feb 2023 · FDA Enforcement Report
Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit recalled
GFA Production Xiamen Co is recalling Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid, 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
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-0249-2023
- 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
- Drug class
- Creams, Ointments & Gels
Timeline
| 23 Dec 2022 | Recall initiated by company | |
| 27 Jan 2023 | Classified by FDA | +35 days |
| 8 Feb 2023 | Published 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
Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2128
Where it was distributed
Nationwide and Canada.
Questions about this recall
Is Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid recalled?
Yes. GFA Production Xiamen Co recalled Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid on 23 Dec 2022. The recall is Class I and its status is Terminated. Recall number D-0249-2023.
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 #: W05L28, exp 12/28/2023; W06F10, exp 06/10/2024; 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.
More recalls from GFA Production Xiamen Co
All 10| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Easy Care first aid Burn Cream recalled by GFA Production Xiamen Co | GFA Production Xiamen Co | Sterility | Nationwide |
| Drug | CLASS I | Adventure First Aid 0, First Aid Kit recalled | GFA Production Xiamen Co | Sterility | Nationwide |
| Drug | CLASS I | Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit recalled | GFA Production Xiamen Co | Sterility | Nationwide |
| Drug | CLASS I | Easy Care First Aid 25 Person 2009 ANSI, First Aid Kit recalled | GFA Production Xiamen Co | Sterility | Nationwide |
| Drug | CLASS I | CVS First Aid Home, First Aid Kit recalled by GFA Production Xiamen Co | GFA Production Xiamen Co | Sterility | Nationwide |