Atlas FDA

Allez Medical Applications, Inc. 4Closure Surgical Fascia Closure System , Catalog ref. 4S. Sterile, One Time Use, Conte

FDA device recall Z-1085-2007 · posted 2007-07-24 · Terminated

Recall details

Recalling firm
Synovis Surgical Inovation Div. of
Reason for recall
There is a potential for the pouch to become damaged during shipping, compromising the sterility of the device inside.
Action taken
Consignees were sent a letter on June 19, 2007. The letter identified the product and problem. The letter also included a form for inventory purposes which is to be completed and faxed to Synovis.
Root cause
Other
Status
Terminated
Product code
GDF
Quantity affected
1box (4 untis)
Distribution
Nationwide.
Date initiated
2007-06-19
Date posted
2007-07-24
Date terminated
2012-05-08
Location
Saint Paul, MN

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