Device recall
Z-0458-2010: Nonin Model 7600B cerebral oximeter pod. Used with the Nonin Model 7600 Regional…
FDA device recall · Class II · Nonin Medical, Inc
Key facts
| Recall number (Z-number) | Z-0458-2010 |
|---|---|
| Recall event | 53801 |
| Product | Nonin Model 7600B cerebral oximeter pod. Used with the Nonin Model 7600 Regional Oximeter with Equanox Technology and Bluetooth Wireless Technology. Nonin Medical, Inc., 13700 First Avenue North, Plymouth, Minnesota 55441-5443 USA. |
| Product code | MUD |
| Recalling firm | Nonin Medical, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 29, 2012 |
| 510(k) numbers | K090807 |
| FEI number | 2183646 |
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