Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IF 8000 Recalled by Zynex Medical, Inc. Due to Zynex notified customers that a malfunction in the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zynex Medical, Inc. directly.
Affected Products
IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulation) mode. Designed for use in physical therapy, rehabilitation, and pain relief applications.
Quantity: 1,461
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zynex Medical, Inc.
Zynex Medical, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report