Cenorin ThermaSure Medical Device Drying Cabinet, series 130 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ThermaSure Medical Device Drying Cabinet, series 130
Brand
Cenorin
Lot Codes / Batch Numbers
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.
Products Sold
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.
Cenorin is recalling ThermaSure Medical Device Drying Cabinet, series 130 due to Potential for user to receive an electrical shock.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for user to receive an electrical shock.
Recommended Action
Per FDA guidance
Letter dated 12/20/2006 notifying customers of potential shock hazard under certain fault conditions and that a corrective action upgrade is being developed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026