FDA Medical Device Recalls (openFDA)
Endocare Inc: SurgiFrost Cryosurgical Probes
- Recall number
- Z-0728-03
- Recalling firm
- Endocare Inc
- Product
- SurgiFrost Cryosurgical Probes
- Status
- Terminated
- Initiated
- 2002-10-25
- Posted
- 2003-04-16
- Terminated
- 2003-04-15
- Reason
- Device design failure, connectivity.
- Root cause
- Other
- Action
- This recall has been completed. Recall notice was sent by fax on October 25, 2002.
- Quantity
- 933
- Distribution
- Product was sent only to one Canadian distribution company whoin turn sold it internationally and back to the USA.
- Lot, serial or model codes
- Lots 02-0464; 02-0474; 02-0578; 02-0711; 02-0852; 02-0911; 02-0981; 02-0982
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GEH
- Firm FEI
- 3008262715
- Firm city
- Irvine
- Firm state
- CA
- 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