FDA Recall
Terminated
Synergraft CryoValve, Aortic Valve & Conduit SG
Recall: Z-0528-04
·
Initiated January 16, 2004
Recall
- Recall Number
- Z-0528-04
- Event Number
- 28176
- Firm
- Cryolife Inc
- FEI Number
- 3001451326
- Product Code
- MIE
- Status
- Terminated
- Root Cause
- Other
- Initiated
- January 16, 2004
- Posted
- July 20, 2004
- Terminated
- September 3, 2004
- Address
- 1655 Roberts Blvd Nw, Kennesaw, GA, 30144-3632
Description
Synergraft CryoValve, Aortic Valve & Conduit SG
Reason
Microorganisms were detected in associated tissue.
Action
Consignees were notified by letter on 1/16/2004.
Distribution
CA, MI,OK
Quantity
1 unit