FDA Medical Device Recalls (openFDA)
Cenorin: ThermaSure Medical Device Drying Cabinet, series 1000
- Recall number
- Z-0713-2007
- Recalling firm
- Cenorin
- Product
- ThermaSure Medical Device Drying Cabinet, series 1000
- Status
- Terminated
- Initiated
- 2006-12-21
- Posted
- 2007-04-04
- Terminated
- 2007-11-09
- Reason
- Potential for user to receive an electrical shock.
- Root cause
- Other
- Action
- Letter dated 12/20/2006 notifying customers of potential shock hazard under certain fault conditions and that a corrective action upgrade is being developed.
- Quantity
- 8 units
- Distribution
- Worldwide.
- Lot, serial or model codes
- Catalog #s 090010-02, 090010-04, 090011-00, 090011-02. Serial Numbers: 100401, 100402, 100403, 100404, 100501, 100601, 100602, 100603
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LDS
- Firm FEI
- 3004153171
- Firm city
- Kent
- Firm state
- WA
- 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