FDA Device Recalls

Recalls /

#98939

Product

Argon Medical Devices Arterial Line Kit/1 20ga x 6", Part Number 498100, Lots 99767185, 99767266, and 99768223 Multi-purpose Kit blister tray coupled with Tyvek lid stock heat-sealed to form a sterile barrier

FDA product code
FTNPlastic Surgery And Accessories Kit
Device class
Class 1
Medical specialty
General, Plastic Surgery
Affected lot / code info
Lots 99767185, 99767266, and 99768223

Why it was recalled

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

Root cause (FDA determination)

Other

Action the firm took

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.

Recalling firm

Firm
Argon Medical Devices, Inc
Address
1445 Flat Creek Rd, Athens, Texas 75751

Distribution

Distribution pattern
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

Timeline

Recall initiated
2011-03-14
Posted by FDA
2011-04-27
Terminated
2012-04-24
Status

Source: openFDA Device Recall endpoint. Recall record ID #98939. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.