Cryolife Inc began a recall of CryoValve, Pulmonary Valve & Conduit on . The reason FDA records is "Additional serological testing performed after distribution indicates the donor has a past Hepatitis B infection". As of , the recall status on record is Terminated.
Recall record
- Recall number
- Z-0480-06
- Status
- Terminated
- Initiated
- Posted
- Terminated
- Recalling firm
- Artivion, Inc.
- Product
- CryoValve, Pulmonary Valve & Conduit
- Product code
- MIE Heart-Valve, Allograft
- Reason for recall
- Additional serological testing performed after distribution indicates the donor has a past Hepatitis B infection.
- FDA root cause
- Other
- Action
- Physicians were notified by letter on 1/27/2006.
- Quantity in commerce
- 1 unit
- Distribution
- NY
- Product codes and lots
- Donor number 78142, Serial number 8306247, Model number PV00
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
