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FDA Medical Device Recalls (openFDA)

First Aid Only Inc: First Aid kits, First Aid Only brand, containing various products to include acetaminophen and other first aid supplies, various sizes, - travel size, all purpose, first aid response kit, on-the-road, recreational, outdoor. First Aid Only, Inc. Vancouver, WA

Recall number
Z-0145-2007
Recalling firm
First Aid Only Inc
Product
First Aid kits, First Aid Only brand, containing various products to include acetaminophen and other first aid supplies, various sizes, - travel size, all purpose, first aid response kit, on-the-road, recreational, outdoor. First Aid Only, Inc. Vancouver, WA
Status
Terminated
Initiated
2006-08-17
Posted
2006-11-02
Terminated
2011-04-08
Reason
Kits contain acetaminophen tablets that were recalled due to being contaminated with mold.
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
365,298 total kits of all brands
Distribution
Kits were distributed nationwide to distributors, retailers and to one international distributor.
Lot, serial or model codes
Kit codes C-0054, C-0094, C-0104, C-0114, C-0124, C-0154, C-0164, C-0174, C-0184, C-0194, C-0224, C-0234, C-0244, C-0294, C-0304, C-0294, C-0164, B-0264, C-0314, C-0104, C-0224, C-0314, C-0104, C-0294, D-0024, D-0064, D-0084, D-0134, D-0264, C-0104, C-0094, E-0134, F-0074, G-0194  Acetaminophen coded 03M847, expiration 12/06
510(k) numbers
not on file
PMA numbers
not on file
Product code
LRR
Firm FEI
3023917
Firm city
Vancouver
Firm state
WA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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