Device recall
Z-0004-2016: Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
FDA device recall · Class II · Lifeline Systems, Incorporated
Key facts
| Recall number (Z-number) | Z-0004-2016 |
|---|---|
| Recall event | 71858 |
| Product | Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System. |
| Product code | ILQ |
| Recalling firm | Lifeline Systems, Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 10, 2020 |
| 510(k) numbers | K914103 |
| FEI number | 1000086682 |
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