Zynex Medical, Inc. recalls IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulation) mode. Designe

Recalled July 2, 2014 · FDA recall Z-1874-2014 · Zynex Medical

Hazard

Zynex notified customers that a malfunction in the IF 8000 can result in the device ceasing to operate, and in some instances,overheating and becoming hot to the touch. · FDA Class II

Units

1,461

Sold at

Nationwide Distribution

Description

Zynex notified customers that a malfunction in the IF 8000 can result in the device ceasing to operate, and in some instances,overheating and becoming hot to the touch.

Product

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

Manufacturer(s)

Zynex Medical, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →