Device recall
Z-1913-2018: Philips HeartStart FRx AED.
FDA device recall · Class II · Philips Electronics North America Corp.
Key facts
| Recall number (Z-number) | Z-1913-2018 |
|---|---|
| Recall event | 79343 |
| Product | Philips HeartStart FRx AED. |
| Product code | MKJ |
| Recalling firm | Philips Electronics North America Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 19, 2020 |
| 510(k) numbers | K050004 |
| FEI number | 1000524572 |
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