Atlas FDA

Micro-temp II heat therapy unit, model #747.

FDA device recall Z-0671-05 · posted 2005-04-06 · Terminated

Recall details

Recalling firm
Cincinnati Sub-Zero Products Inc
Reason for recall
There is the potential that the power switch assembly can dislodge from the cabinet during use.
Action taken
The recalling firm sent letters, dated 1/18/04.
Root cause
Other
Status
Terminated
Product code
ILO
Quantity affected
553 devices.
Distribution
The product was distributed to hospitals throughout the United States.
Date initiated
2005-01-18
Date posted
2005-04-06
Date terminated
2007-09-21
Location
Cincinnati, OH

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