Device recall
Z-2105-2011: Inter x 5002 Device, Inter x Professional Sport Device, Inter x 1000 Personal…
FDA device recall · Class II · Neuro Resource Group Inc
Key facts
| Recall number (Z-number) | Z-2105-2011 |
|---|---|
| Recall event | 58255 |
| Product | Inter x 5002 Device, Inter x Professional Sport Device, Inter x 1000 Personal Device, and Inter x Personal Sport packaged with Triad alcohol wipes. The alcohol wipes manufactured by the Triad Group were labeled under brand names Triad, Select, Select Medical Products, PSS Select or PSS World Medical… |
| Product code | GZJ |
| Recalling firm | Neuro Resource Group Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 23, 2011 |
| 510(k) numbers | K042912 |
| FEI number | 3004786509 |
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