Device recall
Z-0268-2018: Philips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare…
FDA device recall · Class III · Philips Electronics North America Corporation
Key facts
| Recall number (Z-number) | Z-0268-2018 |
|---|---|
| Recall event | 78733 |
| Product | Philips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare environments and transport within a facility. |
| Product code | MHX |
| Recalling firm | Philips Electronics North America Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 17, 2020 |
| 510(k) numbers | K112652 |
| 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