Device recall
Z-2604-2016: CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's…
FDA device recall · Class II · INNOKAS MEDICAL OY
Key facts
| Recall number (Z-number) | Z-2604-2016 |
|---|---|
| Recall event | 74884 |
| Product | CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care. |
| Product code | MWI |
| Recalling firm | INNOKAS MEDICAL OY |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2017 |
| 510(k) numbers | K133810 |
| FEI number | 3007615597 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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