Medical DeviceOct 7, 2015
Lifeline Systems Philips GoSafe Mobile Help Button recall — FDA Z-0004-2016
Irregular battery disconnection resulted in issues with Mobile Health Button (MHB) Charging.
Class IIFDA: TerminatedLifeline Systems, Inc.
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceJul 15, 2015
Lifeline Systems Philips GoSafe Communicator 7000L Personal emergency response system recall — FDA Z-1987-2015
Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.
Class IIFDA: TerminatedLifeline Systems, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Lifeline Systems, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.