Device recall
Z-0373-2010: SureSigns Vital Signs Monitors (VS3)-Vital Signs Viewer Central Viewing Station…
FDA device recall · Class II · Philips Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-0373-2010 |
|---|---|
| Recall event | 53688 |
| Product | SureSigns Vital Signs Monitors (VS3)-Vital Signs Viewer Central Viewing Station View up to 12 VM monitors at 1 time Part number: 863069,863070,863071,863072,863073,863074,453564041251,453564041261, 453564041271,453564041281,453564041291, 453564041301 The SureSigns VM3, VM4, VM6, VM8 and VS3 monitors… |
| Product code | MHX |
| Recalling firm | Philips Healthcare Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 20, 2013 |
| 510(k) numbers | K070588 |
| FEI number | 1218950 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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