Lifeline Systems, Incorporated: Medical Device Recall in 2015 - (Recall #: Z-1987-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Philips GoSafe Communicator 7000L Personal emergency response system.

Product Classification:

Class II

Date Initiated: April 22, 2015

Date Posted: July 15, 2015

Recall Number: Z-1987-2015

Event ID: 71208

Reason for Recall:

Home communicator Model 7000L may not sense the phone line under certain unusual landline phone conditions.

Status: Terminated

Product Quantity: 3189 devices total, 38 are subject to recall

Code Information:

Serial Numbers: 9030003931 9030001761 9030002025 9030002242 9030001588 9030000853 9030001696 9030003178 9030003086 9030000589 9030001526 9030003837 9030000681 9030003507 9030000600 9030001060 9030001517 9030004154 9030002875

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated