Device recall
Z-1917-2010: Automated External Defibrillator (AED) of brand name "Philips HeartStart HS1…
FDA device recall · Class II · Philips Medical Systems
Key facts
| Recall number (Z-number) | Z-1917-2010 |
|---|---|
| Recall event | 55579 |
| Product | Automated External Defibrillator (AED) of brand name "Philips HeartStart HS1 Home" (Model Number M5068A). Device is designed for use on a person in sudden cardiac arrest who is unresponsive when shaken and not breathing normally |
| Product code | MKJ |
| Recalling firm | Philips Medical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 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