Device recall
Z-2892-2018: Philips SureSigns VSV (Vital Signs Viewer), 863067 Indicated for central…
FDA device recall · Class II · Philips Electronics North America Corporation
Key facts
| Recall number (Z-number) | Z-2892-2018 |
|---|---|
| Recall event | 80645 |
| Product | Philips SureSigns VSV (Vital Signs Viewer), 863067 Indicated for central monitoring of multiple adult, pediatric and neonatal patients, and where the clinician decides to monitor cardiac arrhythmia of adult, pediatric and neonatal patients to gain information for the treatment, to monitor adequacy… |
| Product code | MHX |
| Recalling firm | Philips Electronics North America Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 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