Device recall
Z-1911-2008: Phillips Medical Systems, SureSigns VS3 Vital Signs Monitor model numbers…
FDA device recall · Class II · Philips Medical Systems
Key facts
| Recall number (Z-number) | Z-1911-2008 |
|---|---|
| Recall event | 47886 |
| Product | Phillips Medical Systems, SureSigns VS3 Vital Signs Monitor model numbers 863071, 863072, 863073, 863074. All four model numbers have the same user manual. The device is intended for monitoring, recording and alarming of multiple physiological parameters. |
| Product code | MHX |
| Recalling firm | Philips Medical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 29, 2017 |
| 510(k) numbers | K052707 |
| 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