FDA Medical Device Recalls (openFDA)
Lifeline First Aid LLC: Wilderness First Aid Kit, Part Number 4120; UPC 0-91966-04120-6, contains 110 Pieces. The kit is labeled in parts: "***WILDERNESS FIRST AID KIT***MODEL 4120*** 2 IODINE PREP PADS***Lifeline First Aid, LLC***Wilsonville, OR 97070, USA***www.lifelinefirstaid.com***". First aid kit.
- Recall number
- Z-0123-2012
- Recalling firm
- Lifeline First Aid LLC
- Product
- Wilderness First Aid Kit, Part Number 4120; UPC 0-91966-04120-6, contains 110 Pieces. The kit is labeled in parts: "***WILDERNESS FIRST AID KIT***MODEL 4120*** 2 IODINE PREP PADS***Lifeline First Aid, LLC***Wilsonville, OR 97070, USA***www.lifelinefirstaid.com***". First aid kit.
- Status
- Terminated
- Initiated
- 2011-07-07
- Posted
- 2011-10-27
- Terminated
- 2012-03-29
- Reason
- The first aid kits are recalled because the kits contain Iodine Prep Pad single use wipes which were recalled by Triad.
- Root cause
- Material/Component Contamination
- Action
- Lifeline First Aid, LLC sent a " PRODUCT RECALL NOTICE-LIFELINE FIRST AID KITS WHICH INCLUDE H & P [TRIAD] PVP IODINE WIPES" letter dated July 7, 2011 to all affected customers. The letter states that Lifeline First Aid, LLC has become aware of a recall of Povidone Iodine Wipes manufactured by H&P Industries Inc. (TRIAD GROUP) and marketed under various brand names, including Triad and Swift. The recall of the Povidone Iodine Wipe is due to potential microbial contamination of the product. The letter instructs customers to collect and quarantine all affected products and to complete and return an attached Customer Response Form via fax to (503) 783-3721. Affected products will be replaced without charge and acceptable Lifeline first aid kits will be re-worked and returned using Lifeline's standard RGA process. Customers may call Lifeline customer service at 1 (877) 377-8243 for further instructions.
- Quantity
- 1800 kits
- Distribution
- Nationwide Distribution
- Lot, serial or model codes
- no codes.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LRR
- Firm FEI
- 3002714597
- Firm city
- Wilsonville
- Firm state
- OR
- 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
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
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