Date Initiated by Firm | July 07, 2011 |
Date Posted | October 27, 2011 |
Recall Status1 |
Terminated 3 on March 29, 2012 |
Recall Number | Z-0121-2012 |
Recall Event ID |
60041 |
Product Classification |
First aid kit with drug - Product Code LRR
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Product | Highlands First Aid Kit, Part Number 4116, UPC 0-91966-04116-9, contains 65 Pieces.
The kit is labeled in parts: "***HIGHLANDS FIRST AID KIT***MODEL 4166***
1 IODINE PREP PADS***Lifeline First Aid, LLC***Wilsonville, OR 97070, USA***www.lifelinefirstaid.com***".
First aid kit. |
Code Information |
no codes. |
Recalling Firm/ Manufacturer |
Lifeline First Aid LLC 26200 SW 95th Ave Ste 301 Wilsonville OR 97070-8204
|
For Additional Information Contact | Bryan O'Doherty 503-783-3653 |
Manufacturer Reason for Recall | The first aid kits are recalled because the kits contain Iodine Prep Pad single use wipes which were recalled by Triad. |
FDA Determined Cause 2 | 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 in Commerce | 17,460 kits |
Distribution | Nationwide Distribution |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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