CLASS II Device recall · Reported 11 May 2022 · FDA Enforcement Report

First Aid Kits containing acetaminophen under brand names recalled

ASO is recalling First Aid Kits containing acetaminophen under brand names Equate (Walmart), Meijer, and, distributed nationwide in the US. The recall was initiated on 2 Mar 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesProduct distributed in first kits under the following names/codes: 1) Equate (Walmart) - FIRST AID KIT 140 PIECES, SKU #s 566904301 and 567925067 - contains acetaminophen with Pouch lot #6132 (expired 09/2021). Kit was sold under ASO Item Nos: a) 187619: Lots 00106279 (EXP 4/1/2021); 00106525 (EXP 6/1/2020); 00106615 (EXP 3/1/2021); 00108538 (EXP 3/1/2021); 19252 (EXP.9/1/2021); and 19253 (EXP.9/1/2021) b) 188583: Lots 00106926 (EXP 6/1/2020); 00107119 (EXP 3/1/2021); 00108453 (EXP 3/1/2021); 00106615 (EXP 3/1/2021), and 00108538 (EXP 3/1/2021). 2) Meijer - FIRST AID KIT 150 PIECES, SKU #4212608-024-002 - contains acetaminophen with Pouch lot #6132 (expired 09/2021). Kit was sold under ASO Item No. 189099, Lot #00107831 (EXP 10/01/2020) 3) Care Science (Amazon) - FIRST AID KIT 200 PIECES, SKU #B07CQBNWQY - contains acetaminophen with Pouch lot #6132 (expired 09/2021). Kit was sold under ASO Item No. #188819, Lot #00112542 (EXP 06/01/2021).

Quantity recalled73,668 kits

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1031-2022
FDA event ID: 89824
Recalling firm: ASO, Sarasota, FL
Brand: acetaminophen under
Classification: Class II
Status: Terminated
Recall initiated: 2 Mar 2022
FDA classified: 4 May 2022
Reported: 11 May 2022
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

2 Mar 2022	Recall initiated by company
4 May 2022	Classified by FDA	+63 days
11 May 2022	Published 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

Kits contained recalled acetaminophen.

Product as listed by the FDA

First Aid Kits containing acetaminophen under brand names Equate (Walmart), Meijer, and Care Science (Amazon)

Where it was distributed

US Nationwide distribution.

Nationwide

Stores named: Walmart, Amazon, Meijer, Online Retailers

Questions about this recall

Why was it recalled?

Kits contained recalled acetaminophen.

Which lots are affected?

Product distributed in first kits under the following names/codes: 1) Equate (Walmart) - FIRST AID KIT 140 PIECES, SKU #s 566904301 and 567925067 - contains acetaminophen with Pouch lot #6132 (expired 09/2021). Kit was sold under ASO Item Nos: a) 187619: Lots 00106279 (EXP 4/1/2021); 00106525 (EXP 6/1/2020); 00106615 (EXP 3/1/2021); 00108538 (EXP 3/1/2021); 19252 (EXP.9/1/2021); and 19253 (EXP.9/1/2021) b) 188583: Lots 00106926 (EXP 6/1/2020); 00107119 (EXP 3/1/2021); 00108453 (EXP 3/1/2021); 00106615 (EXP 3/1/2021), and 00108538 (EXP 3/1/2021). 2) Meijer - FIRST AID KIT 150 PIECES, SKU #4212608-024-002 - contains acetaminophen with Pouch lot #6132 (expired 09/2021). Kit was sold under ASO Item No. 189099, Lot #00107831 (EXP 10/01/2020) 3) Care Science (Amazon) - FIRST AID KIT 200 PIECES, SKU #B07CQBNWQY - contains acetaminophen with Pouch lot #6132 (expired 09/2021). Kit was sold under ASO Item No. #188819, Lot #00112542 (EXP 06/01/2021).

Where was it sold?

US Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

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 26 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 ASO

All 15

Reported	Class	Recall	Company	Reason	Where
10 May 2023Device	CLASS II	Walgreens Bandages recalled by ASO	ASO	Packaging Defects	Nationwide
24 Aug 2022Device	CLASS II	CVS Health Sterile Surgical Pads, Cushion Comfort, packaged 12 pads recalled	ASO	Packaging Defects	Nationwide
12 Dec 2018Device	CLASS II	Family Wellness First Aid Sterile Gauze Pad White, bleached recalled	ASO	Device Malfunction	Nationwide
2 Sep 2015Device	CLASS II	Carepak Sheer Adhesive Bandages 50 Sterile Bandages Assorted Sizes recalled	ASO	Other	RI
9 Oct 2013Device	CLASS II	Shopko Waterproof Adhesive Pads Antibacterial recalled by ASO	ASO	Other	IN, NE, WI

Other Other Medical Devices recalls

All 13,908

Reported	Class	Recall	Company	Reason	Where
14 Oct 2026Device	CLASS II	Plastics Tray kits recalled by Avid Medical	Avid Medical	Foreign Material	Nationwide
14 Oct 2026Device	CLASS II	Heart Prep Tray kits recalled by Avid Medical	Avid Medical	Other	Nationwide
14 Oct 2026Device	CLASS II	Pack Open Heart Cfh kits recalled by Avid Medical	Avid Medical	Other	Nationwide
14 Oct 2026Device	CLASS II	Sperm Ab Elisa (96 well plate test) recalled by DRG International	DRG International	Other	Nationwide
14 Oct 2026Device	CLASS III	BeneView Series recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide