ThermaSure Medical Device Drying Cabinet, series 1000
FDA Recall Z-0713-2007 · Posted 2007-04-04
Recalling FirmCenorin
Recall StatusTerminated
Product CodeLDS
Date Initiated2006-12-21
Date Terminated2007-11-09
Product Quantity8 units
Reason for Recall
Potential for user to receive an electrical shock.
Firm 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.
Root Cause
Other
Distribution Pattern
Worldwide.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.