IF 8000 — Class II medical device recall Z-1874-2014
Terminated recall by Zynex Medical, Inc., reported 2014-07-02, distributed nationwide. Zynex notified customers that a malfunction in the IF 8000 can result in the device ceasing to operate, and in
| Recall number | Z-1874-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zynex Medical, Inc., Lone Tree, CO, United States |
| Recall initiated | 2009-01-25 |
| Classified | 2014-06-26 |
| Reported by FDA | 2014-07-02 |
| Terminated | 2015-07-02 |
| Distributed | Nationwide (US) |
| Quantity | 1,461 |
| Reason classes | device malfunction |
| Serial numbers | 2483901, 2483906, 2483929, 2483932, 2483935, 2483944, 2483950, 2483964, 2483965, 2483970, 2483985, 2483992, 2484004, 2484006, 2484007, 2484014, 2484018, 2484036, 2484041, 2484048, 2484070, 2484071, 2484077, 2484079, 2484090 and 475 more |
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.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1874-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.