Cryolife Inc CryoValve, Aortic Valve and Conduit Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CryoValve, Aortic Valve and Conduit
Brand
Cryolife Inc
Lot Codes / Batch Numbers
Donor #56844, Serial #7399626, Model #AV00
Products Sold
Donor #56844, Serial #7399626, Model #AV00
Cryolife Inc is recalling CryoValve, Aortic Valve and Conduit due to An incorrect lot number was entered in the production record for the solution in which this allograft was packaged.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
An incorrect lot number was entered in the production record for the solution in which this allograft was packaged.
Recommended Action
Per FDA guidance
Consignee was notified by letter on 12/02/2004.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
TN
Page updated: Jan 10, 2026