Z-0147-2007

First Aid Kit, Nexcare brand, all purpose first aid kit containing acetaminophen and a variety of first aid...

Name: Z-0147-2007 First Aid Kit, Nexcare brand, all purpose first aid kit containing acetaminophen and a variety of first aid...
Creator: First Aid Only Inc
Published: 2006-08-17
License: https://open.fda.gov/license/

Acme United Corp. / initiated 2006-08-17 / Terminated

FDA source

First Aid Only Inc began a recall of First Aid Kit, Nexcare brand, all purpose first aid kit containing acetaminophen and a variety of first aid supplies. Made in U.S.A. for 3M 3M Consumer Health... on 2006-08-17. The reason FDA records is "Kits contain acetaminophen tablets that were recalled due to being contaminated with mold". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0147-2007
Status: Terminated
Initiated: 2006-08-17
Posted: 2006-11-02
Terminated: 2011-04-08
Recalling firm: Acme United Corp.
Product: First Aid Kit, Nexcare brand, all purpose first aid kit containing acetaminophen and a variety of first aid supplies. Made in U.S.A. for 3M 3M Consumer Health Care St. Paul, MN 55144-1000
Product code: LRR First Aid Kit With Drug
Reason for recall: Kits contain acetaminophen tablets that were recalled due to being contaminated with mold.
FDA root cause: Other
Action: The firm issued a letter dated August 17, 2006 to their customers advising of the recall and requesting product be removed from retail level and returned to the firm.
Quantity in commerce: 365,298 total kits of all brands
Distribution: Kits were distributed nationwide to distributors, retailers and to one international distributor.
Product codes and lots: Kit code C-0234, C-0244, C-0254, C-0264 Acetaminophen coded 03M847, expiration 12/06

Product code LRR

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)