FDA Recall Terminated

Argon Medical Devices, Arterial Line Kit, Arterial Catheter Mini Kit 20gax6in, Part Number 498101, Lot 99767264 Multi-purpose Kit blister tray coupled with Tyvek lid stock heat-sealed to form a sterile barrier.

Recall: Z-2089-2011 · Initiated March 14, 2011

Recall

Recall Number
Z-2089-2011
Event Number
58289
Firm
Argon Medical Devices, Inc
FEI Number
1625425
Product Code
FTN
Status
Terminated
Root Cause
Other
Initiated
March 14, 2011
Posted
April 27, 2011
Terminated
April 24, 2012
Address
1445 Flat Creek Rd, Athens, TX, 75751

Description

Argon Medical Devices, Arterial Line Kit, Arterial Catheter Mini Kit 20gax6in, Part Number 498101, Lot 99767264 Multi-purpose Kit blister tray coupled with Tyvek lid stock heat-sealed to form a sterile barrier.

Reason

Packaging for sterile tray has the potential to have a hole which could compromise sterility for the products inside.

Action

Argon Medical Devices sent an Urgent Medical Device Recall letter dated March 14, 2011, by certified mail to all affected consignees. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to identify, quarantine and return any product remaining at their facility utilizing the instruction on the 2011 Tray Recall Response Form. Customers were instructed to complete the response form included with the letter and return by fax or email as indicated as soon as possible. Customers were instructed to pass the notice on to all those who need to be aware within their organization or to any organization where the potentially affected devices have been transferred. For questions regarding this recall call (903) 677-9375.

Distribution

Worldwide Distribution - USA including AL, AZ, CA, CO, DE, GA, HI, IL, IN, LA, MD, MN, ND, NE, NH, NJ, NY, OK, PA, SC, TX, VA, WA, and WI and the countries of Nationwide, Japan, Australia, Canada, Singapore, and the Netherlands

Quantity

440 units