Device recall
Z-0817-2016: MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation)…
FDA device recall · Class II · Nihon Kohden America Inc
Key facts
| Recall number (Z-number) | Z-0817-2016 |
|---|---|
| Recall event | 73114 |
| Product | MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stimulator Box) JB-116B, JB-132B (Amplifiers) Electromyography. (EMG) |
| Product code | GWF |
| Recalling firm | Nihon Kohden America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 22, 2016 |
| 510(k) numbers | K051178 |
| FEI number | 2080783 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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