Device recall
Z-2167-2011: Philips NM3 Monitors, Model 7900 PHILIPS NM3 Monitor, English - P/N 1051674…
FDA device recall · Class II · Respironics Novametrix, LLC.
Key facts
| Recall number (Z-number) | Z-2167-2011 |
|---|---|
| Recall event | 57594 |
| Product | Philips NM3 Monitors, Model 7900 PHILIPS NM3 Monitor, English - P/N 1051674 PHILIPS NM3 Monitor, English Refurbished - P/N U1051674 PHILIPS NM3 Monitor, English, Demo Unit - P/N DU1051674 PHILIPS NM3 Monitor, Spanish - P/N 1060462 NM3 is a multi-parameter patient monitor that utilizes the FloTrak… |
| Recalling firm | Respironics Novametrix, LLC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2013 |
| 510(k) numbers | K080652, K091459, K092217 |
| FEI number | 1219324 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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