Philips GoSafe Communicator 7000L Personal emergency response system — Class II medical device recall Z-1987-2015
Terminated recall by Lifeline Systems, Incorporated, reported 2015-07-15, distributed nationwide. Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.
| Recall number | Z-1987-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lifeline Systems, Incorporated, Framingham, MA, United States |
| Recall initiated | 2015-04-22 |
| Classified | 2015-07-06 |
| Reported by FDA | 2015-07-15 |
| Terminated | 2016-08-24 |
| Distributed | Nationwide (US) |
| Serial numbers | 9030000589, 9030000600, 9030000681, 9030000853, 9030001060, 9030001517, 9030001526, 9030001588, 9030001696, 9030001761, 9030002025, 9030002242, 9030002875, 9030003086, 9030003178, 9030003507, 9030003837, 9030003931, 9030004154 |
Product
Philips GoSafe Communicator 7000L Personal emergency response system.
Reason for recall
Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1987-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.