Drug recall
HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator.
FDA recall event 79010 · Class II · Lifeline Systems Company
Key facts
| Event ID | 79010 |
|---|---|
| Recall numbers | Z-1316-2018 |
| Recalling firm | Lifeline Systems Company |
| Product type | Devices |
| Products | HomeSafe AutoAlert Pendant works in conjunction with a compatible Lifeline communicator. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A programing error in some Model FD100 HomeSafe AutoAlert Pendants will render the fall detection feature inoperable. |
| Initiation date | Nov 13, 2017 |
| Report date | Apr 18, 2018 |
| Termination date | May 16, 2019 |
| City | Framingham |
| State | MA |
| Country | United States |
| FEI number | 1000086682 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: