Device recall
Z-1779-2008: Philips defibrillator, model M5066A. Sold in the US by Philips as an OTC under…
FDA device recall · Class II · Philips Medical Systems
Key facts
| Recall number (Z-number) | Z-1779-2008 |
|---|---|
| Recall event | 47833 |
| Product | Philips defibrillator, model M5066A. Sold in the US by Philips as an OTC under the brand name Philips "HeartStart On Site Defibrillator" and outside the U.S. by Philips with the brand name Philips "HeartStart Defibrillator". The HeartStart is an automated external defibrillator for use on site and… |
| Product code | MKJ |
| Recalling firm | Philips Medical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 23, 2012 |
| 510(k) numbers | K020715, K040904 |
| 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