Device recall
Z-2842-2016: HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A
FDA device recall · Class II · Philips Electronics North America Corporation
Key facts
| Recall number (Z-number) | Z-2842-2016 |
|---|---|
| Recall event | 75041 |
| Product | HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A |
| Product code | MKJ |
| Recalling firm | Philips Electronics North America Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 24, 2020 |
| 510(k) numbers | K031187, K040404, K051134, K061707, K062233 |
| 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