Device recall
Z-1708-2017: eCare Coordinator Product Usage: is software intended for use in data…
FDA device recall · Class II · Philips Visicu
Key facts
| Recall number (Z-number) | Z-1708-2017 |
|---|---|
| Recall event | 76660 |
| Product | eCare Coordinator Product Usage: is software intended for use in data aggregation, patient interaction facilitation, storage and clinical information management with independent physiological devices and ancillary systems that are connected either directly or through networks. The software is… |
| Product code | DRG |
| Recalling firm | Philips Visicu |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 27, 2017 |
| 510(k) numbers | K141706 |
| FEI number | 3003063823 |
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