Device recall
Z-0545-2021: Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for…
FDA device recall · Class II · Philips North America Llc
Key facts
| Recall number (Z-number) | Z-0545-2021 |
|---|---|
| Recall event | 86848 |
| Product | Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside of the hospital… |
| Product code | DSI |
| Recalling firm | Philips North America Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 22, 2021 |
| 510(k) numbers | K083517 |
| FEI number | 3016618143 |
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