Cryolife Inc CryoValve Allograft, Aortic Valve & Conduit Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CryoValve Allograft, Aortic Valve & Conduit
Brand
Cryolife Inc
Lot Codes / Batch Numbers
Donor #66810, Device Serial #8100262, Model #AV00
Products Sold
Donor #66810, Device Serial #8100262, Model #AV00
Cryolife Inc is recalling CryoValve Allograft, Aortic Valve & Conduit due to Donor of distributed allograft was diagnosed with dilated/ischemic cardiomyopathy.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Donor of distributed allograft was diagnosed with dilated/ischemic cardiomyopathy.
Recommended Action
Per FDA guidance
The hospital was notified by letter on 5/05/2003.
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
CA, IN
Page updated: Jan 10, 2026