Device recall
Z-1440-2012: Synaptic 3600 and 3800 with Cranial Electrical Stimulation manufactured by…
FDA device recall · Class II · Synaptic Corp
Key facts
| Recall number (Z-number) | Z-1440-2012 |
|---|---|
| Recall event | 49410 |
| Product | Synaptic 3600 and 3800 with Cranial Electrical Stimulation manufactured by Synaptic USA, Aurora, CO. Transcutaneous nerve stimulation for pain relief and other medical treatment uses. |
| Product code | GZJ |
| Recalling firm | Synaptic Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2012 |
| FEI number | 1000117338 |
At a glance
- None 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