Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-0480-06

CryoValve, Pulmonary Valve & Conduit

Artivion, Inc. / initiated 2006-01-27 / Terminated

Cryolife Inc began a recall of CryoValve, Pulmonary Valve & Conduit on . The reason FDA records is "Additional serological testing performed after distribution indicates the donor has a past Hepatitis B infection". As of , the recall status on record is Terminated.

Recall record

Recall number
Z-0480-06
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Artivion, Inc.
Product
CryoValve, Pulmonary Valve & Conduit
Product code
MIE Heart-Valve, Allograft
Reason for recall
Additional serological testing performed after distribution indicates the donor has a past Hepatitis B infection.
FDA root cause
Other
Action
Physicians were notified by letter on 1/27/2006.
Quantity in commerce
1 unit
Distribution
NY
Product codes and lots
Donor number 78142, Serial number 8306247, Model number PV00