FDA Device recall Z-1987-2015
Philips GoSafe Communicator 7000L Personal emergency response system
- FDA Device
- Class II
- terminated
- Published 2015-07-15
On 2015-07-15 the FDA classified a Class II recall of Philips GoSafe Communicator 7000L Personal emergency response system by Lifeline Systems, citing home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1987-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-04-22 |
| Published | 2015-07-15 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Lifeline Systems |
| Distribution | US |
Product
Philips GoSafe Communicator 7000L Personal emergency response system.
Reason
Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.
Identifiers
| code_info | Serial Numbers: 9030003931 9030001761 9030002025 9030002242 9030001588 9030000853 9030001696 9030003178 903000…Serial Numbers: 9030003931 9030001761 9030002025 9030002242 9030001588 9030000853 9030001696 9030003178 9030003086 9030000589 9030001526 9030003837 9030000681 9030003507 9030000600 9030001060 9030001517 9030004154 9030002875 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1987-2015%22
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