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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:175307

Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature management Model 233 - Product Usage: The system is composed of a heater, a compressor, a circulating pump and blankets/pads.

Official recall number

Z-0417-2020

Evidence summary

Product code
DWJ
Recall status
Terminated
Event initiated
July 02, 2019
Root cause
Labeling False and Misleading
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-0417-2020

Field note

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