Device recall
Z-1874-2014: IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular…
FDA device recall · Class II · Zynex Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1874-2014 |
|---|---|
| Recall event | 68447 |
| 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. |
| Product code | IPF |
| Recalling firm | Zynex Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 2, 2015 |
| 510(k) numbers | K991241 |
| FEI number | 3000214920 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database