FDA Medical Device Recalls (openFDA)
Cenorin: ThermaSure Medical Device Drying Cabinet, series 300
- Recall number
- Z-0712-2007
- Recalling firm
- Cenorin
- Product
- ThermaSure Medical Device Drying Cabinet, series 300
- 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
- 50 units
- Distribution
- Worldwide.
- Lot, serial or model codes
- Catalog #s 090033-02, 090033-04, 090034-02, 090034-04. Serial Numbers: 330304, 330305, 330306, 330307, 330308, 330309, 330310, 330311, 330312, 330313, 330401, 330402, 330403, 340404, 330405, 340406, 330407, 330408, 330409, 330410, 330411, 340412, 330413, 330414, 330415, 330416, 340417, 340501, 330502, 330503, 330504, 330505, 340506, 330507, 330508, 330509, 330510, 330511, 330512, 330601, 330602, 330603, 330604, 330605, 330606, 330607, 330608, 330609, 330610, 330611.
- 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