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U.S. Department of Health and Human Services

Class 2 Device Recall

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 Class 2 Device Recallsee related information
Date Initiated by FirmApril 19, 2004
Date PostedSeptember 28, 2005
Recall Status1 Terminated 3 on January 07, 2008
Recall NumberZ-1590-05
Recall Event ID 32841
Product Classification Heart-Valve, Allograft - Product Code MIE
ProductCryoValve, Aortic Valve & Conduit SG
Code Information Donor #65389, Serial #7943760, SGAV00
Recalling Firm/
Manufacturer		 Cryolife Inc
1655 Roberts Blvd Nw
Kennesaw GA 30144-3632
For Additional Information ContactMr. P. Tyler Cochran, CQA, CTBS
770-419-3355
Manufacturer Reason
for Recall		This recall was initiated as part of the firm's retrospection review of tissues associated with complaints of alleged recipient infection.
FDA Determined
Cause 2		Other
ActionConsignees were notified by telephone and letter on 04/19/2004.
Quantity in Commerce1 tissue
DistributionMO, TX and Sidney Australia
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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