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Terminated

ThermaSure Medical Device Drying Cabinet, series 300

FDA Recall Z-0712-2007 · Posted 2007-04-04

Recalling FirmCenorin
Recall StatusTerminated
Product CodeLDS
Date Initiated2006-12-21
Date Terminated2007-11-09
Product Quantity50 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.

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