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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:127719

IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulation) mode. Designed for use in physical therapy, rehabilitation, and pain relief applications.

Official recall number

Z-1874-2014

Evidence summary

Product code
IPF
Recall status
Terminated
Event initiated
January 25, 2009
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1874-2014