Device recall
Z-0432-2011: Philips HeartStart FRx Defibrillator, Automated External Defibrillator (AED)…
FDA device recall · Class III · Philips Medical Systems
Key facts
| Recall number (Z-number) | Z-0432-2011 |
|---|---|
| Recall event | 49384 |
| Product | Philips HeartStart FRx Defibrillator, Automated External Defibrillator (AED), catalog number 861304. |
| Product code | MKJ |
| Recalling firm | Philips Medical Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 1, 2010 |
| 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