Micro-temp II heat therapy unit, model #747.
FDA Recall Z-0671-05 · Posted 2005-04-06
Recalling FirmCincinnati Sub-Zero Products Inc
Recall StatusTerminated
Product CodeILO
Date Initiated2005-01-18
Date Terminated2007-09-21
Product Quantity553 devices.
Reason for Recall
There is the potential that the power switch assembly can dislodge from the cabinet during use.
Firm Action
The recalling firm sent letters, dated 1/18/04.
Root Cause
Other
Distribution Pattern
The product was distributed to hospitals throughout the United States.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.