Atlas FDA

Part Number 496311, Lot Number 99768100 Multi-purpose Kit blister tray coupled with Tyvek lid stock heat-sealed to form

FDA device recall Z-2086-2011 · posted 2011-04-27 · Terminated

Recall details

Recalling firm
Argon Medical Devices, Inc
Reason for recall
Packaging for sterile tray has the potential to have a hole which could compromise sterility for the products inside.
Action taken
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.
Root cause
Other
Status
Terminated
Product code
FTN
Quantity affected
60 units
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, Sin
Date initiated
2011-03-14
Date posted
2011-04-27
Date terminated
2012-04-24
Location
Athens, TX

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