Cincinnati Sub-Zero Products Hemotherm CE, model 400CE, Heater-Cooling Device recall — FDA Z-1825-2017
Improperly rated fuses were used in the manufacture of the device.
Overview of recall records associated with Cincinnati Sub-Zero Products Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Improperly rated fuses were used in the manufacture of the device.
This page summarizes recall records in which the official source identifies Cincinnati Sub-Zero Products Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.