Lifeline Systems, Incorporated recalls Philips GoSafe Communicator 7000L Personal emergency response system.
- Recall date
- April 22, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1987-2015
- FDA classification
- Class II
- Brand / firm
- Lifeline Systems, Incorporated
- Sold / distributed
- Nationwide Distribution including AK AZ CA CT FL IA IL KY MA MD MT NC NE NH NY OH OR SC VA WA and WI.
Why it was recalled
Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Philips GoSafe Communicator 7000L Personal emergency response system.
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