Atlas FDA

Electri-Cool II

FDA device recall Z-0670-05 · 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 firm sent a recall letter by certified mail, dated 1/18/05, to consignees.
Root cause
Other
Status
Terminated
Product code
ILO
Quantity affected
130 devices
Distribution
The devices were distributed 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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