Z-0711-2007

ThermaSure Medical Device Drying Cabinet, series 130

Name: Z-0711-2007 ThermaSure Medical Device Drying Cabinet, series 130
Creator: Cenorin
Published: 2006-12-21
License: https://open.fda.gov/license/

Cenorin, LLC / initiated 2006-12-21 / Terminated

FDA source

Cenorin began a recall of ThermaSure Medical Device Drying Cabinet, series 130 on 2006-12-21. The reason FDA records is "Potential for user to receive an electrical shock". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0711-2007
Status: Terminated
Initiated: 2006-12-21
Posted: 2007-04-04
Terminated: 2007-11-09
Recalling firm: Cenorin, LLC
Product: ThermaSure Medical Device Drying Cabinet, series 130
Product code: LDS Device, Pasteurization, Hot Water
Reason for recall: Potential for user to receive an electrical shock.
FDA 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 in commerce: 101 units
Distribution: Worldwide.
Product codes and lots: Catalog #s 090035-00, 090035-03, 090036-00, 090036-02. Serial Numbers: 350305, 350306, 350307, 350308, 360309, 350310, 350311, 360312, 350313, 350314, 350401, 350402, 350403, 350404, 350405, 350406, 350407, 350408, 350409, 350410, 350411, 350412, 350413, 350414, 350415, 350416, 350417, 350418, 350419, 350420, 350421, 350422, 350423, 350424, 350425, 350426, 350427, 350501, 360502, 350503, 350504, 350505, 350506, 350507, 350508, 350509, 350510, 350511, 350512, 350513, 350514, 350515, 350516, 350517, 350518, 360519, 350520, 350521, 350522, 350523, 350524, 350525, 350526, 350527, 350528, 350529, 350530, 360531, 350532, 350533, 350534, 350601, 350602, 350603, 350604, 350605, 350606, 350607, 350608, 350609, 350610, 360611, 360612, 350613, 350614, 350615, 350616, 350617, 350618, 350619, 350620, 350621, 350621A, 350622, 350623, 350624, 350625, 350626, 350627, 350628, 350629.

Product code LDS

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)