Device recall
Z-1316-2018: HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline…
FDA device recall · Class II · Lifeline Systems Company
Key facts
| Recall number (Z-number) | Z-1316-2018 |
|---|---|
| Recall event | 79010 |
| Product | HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator. |
| Product code | ILQ |
| Recalling firm | Lifeline Systems Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 16, 2019 |
| 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