FDA Medical Device Recalls (openFDA)
CryoLife, Inc.: Aortic Valve & Conduit
- Recall number
- Z-0842-2007
- Recalling firm
- CryoLife, Inc.
- Product
- Aortic Valve & Conduit
- Status
- Terminated
- Initiated
- 2007-04-17
- Posted
- 2007-06-07
- Terminated
- 2007-12-31
- Reason
- Donor tissue was released prior to information received regarding a pericardial effusion.
- Root cause
- Other
- Action
- Both physicians were contacted by telephone on 4/17 & 18/2007. Both tissues were returned to CryoLife
- Quantity
- 1 tissue
- Distribution
- AZ, CO
- Lot, serial or model codes
- Donor number 87980, Serial number 8892143, Model Number 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