Atlas FDA

Cook brand Zenith AAA Bifurcated main body graft with the H&L-B One-Shot Introducer System, preloaded bifurcated main bo

FDA device recall Z-1175-04 · posted 2004-07-27 · Terminated

Recall details

Recalling firm
Cook, Inc.
Reason for recall
Introducer tubing may contain a vein of unextruded material and carbon black or a strand of tubing material may be displaced from the introducer during use.
Action taken
The firm issued recall letters to customers on 6/10/04. The recall was extended and URGENT EXTENSION OF PRODUCT RECALL notices were sent out on June 23, 2004.
Root cause
Other
Status
Terminated
Product code
MIH
Quantity affected
85
Distribution
Nationwide, Canada, Denmark and Japan.
Date initiated
2004-06-10
Date posted
2004-07-27
Date terminated
2004-11-01
Location
Bloomington, IN

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