FDA Medical Device Recalls (openFDA)
Cryolife Inc: CryoValve, Aortic Valve and Conduit
- Recall number
- Z-0686-05
- Recalling firm
- Cryolife Inc
- Product
- CryoValve, Aortic Valve and Conduit
- Status
- Terminated
- Initiated
- 2004-12-02
- Posted
- 2005-04-06
- Terminated
- 2010-06-28
- Reason
- An incorrect lot number was entered in the production record for the solution in which this allograft was packaged.
- Root cause
- Other
- Action
- Consignee was notified by letter on 12/02/2004.
- Quantity
- 1 tissue
- Distribution
- TN
- Lot, serial or model codes
- Donor #56844, Serial #7399626, Model #AV00
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- MIE
- Firm FEI
- 3001451326
- Firm city
- Kennesaw
- Firm state
- GA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28