Atlas FDA

ThermaSure Medical Device Drying Cabinet, series 1000

FDA device recall Z-0713-2007 · posted 2007-04-04 · Terminated

Recall details

Recalling firm
Cenorin
Reason for recall
Potential for user to receive an electrical shock.
Action taken
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
Status
Terminated
Product code
LDS
Quantity affected
8 units
Distribution
Worldwide.
Date initiated
2006-12-21
Date posted
2007-04-04
Date terminated
2007-11-09
Location
Kent, WA

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