Device recall
Z-2531-2020: Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an…
FDA device recall · Class II · Philips North America, LLC
Key facts
| Recall number (Z-number) | Z-2531-2020 |
|---|---|
| Recall event | 85799 |
| Product | Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No. 867030) or a lntelliVue MMX Multi-Measurement Module (Model No. 867036) |
| Product code | DSI |
| Recalling firm | Philips North America, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 9, 2023 |
| 510(k) numbers | K993383 |
| FEI number | 1218950 |
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