Drug recall
Philips GoSafe Communicator 7000L Personal emergency response system.
FDA recall event 71208 · Class II · Lifeline Systems, Incorporated
Key facts
| Event ID | 71208 |
|---|---|
| Recall numbers | Z-1987-2015 |
| Recalling firm | Lifeline Systems, Incorporated |
| Product type | Devices |
| Products | Philips GoSafe Communicator 7000L Personal emergency response system. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions. |
| Initiation date | Apr 22, 2015 |
| Report date | Jul 15, 2015 |
| Termination date | Aug 24, 2016 |
| 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: