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Terminated

CryoValve, Aortic Valve & Conduit

FDA Recall Z-0530-04 · Posted 2004-07-20

Recalling FirmCryolife Inc
Recall StatusTerminated
Product CodeMIE
Date Initiated2004-01-16
Date Terminated2004-09-03
Product Quantity1 unit

Reason for Recall

Microorganisms were detected in associated tissue.

Firm Action

Consignees were notified by letter on 1/16/2004.

Root Cause

Other

Distribution Pattern

CA, MI,OK

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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