Reported Jul 2, 2014 · Terminated
IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulation) mode. Designed…
Zynex Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Zynex Medical, Inc. · 9990 Park Meadows Dr · Lone Tree, CO · 80124-6739
Is this the product you have?
- IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulation) mode. Designed for use in physical therapy, rehabilitation, and pain relief applications.
- Lot codes and dates
- Serial No
1,461 of 1,461 codes
248390124840062484014248403624840072484018248404824840902484041248398524840792484077248396427892032484071248413824841092484070248395024841612483965248417224840042484164248418324841962484115248434324842282484267248428424841932484336248427224842382484409248392924844412484399248431824844782484422248449124844022484415248442524842042484300248445824845282484567248446424845572484519248459324846022484645248424624846082484714
- Serial No
- Amount recalled
- 1,461
Where it was sold
- Nationwide
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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