Device recall
Z-0608-2020: HeartStart XL+ Defibrillator/Monitor, Model 861290
FDA device recall · Class II · Philips North America, LLC
Key facts
| Recall number (Z-number) | Z-0608-2020 |
|---|---|
| Recall event | 84236 |
| Product | HeartStart XL+ Defibrillator/Monitor, Model 861290 |
| Product code | MKJ |
| Recalling firm | Philips North America, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2023 |
| 510(k) numbers | K110825 |
| 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