Device recall
Z-0419-2010: Philips Lifeline Personal Help Button Pendant Classic and Slimline Style.
FDA device recall · Class II · Philips Lifeline Inc
Key facts
| Recall number (Z-number) | Z-0419-2010 |
|---|---|
| Recall event | 53261 |
| Product | Philips Lifeline Personal Help Button Pendant Classic and Slimline Style. |
| Product code | ILQ |
| Recalling firm | Philips Lifeline Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 2, 2012 |
| 510(k) numbers | K914103 |
| FEI number | 3007138625 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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