Atlas FDA

CryoValve, Pulmonary Valve & Conduit

FDA device recall Z-0774-04 · posted 2004-07-20 · Terminated

Recall details

Recalling firm
Cryolife Inc
Reason for recall
The donor of the tissue had a viral syndrome at the time of death.
Action taken
Consignees were notified by letter on 3/24/2004.
Root cause
Other
Status
Terminated
Product code
MIE
Quantity affected
1 unit
Distribution
CT, PA
Date initiated
2004-03-24
Date posted
2004-07-20
Date terminated
2005-01-19
Location
Kennesaw, GA

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