Physio-Control, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0761-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel in outdoor and indoor emergency care settings within the environmental conditions specified. Product Part Numbers V-15-2-000XXX

Product Classification:

Class II

Date Initiated: March 11, 2010

Date Posted: December 21, 2016

Recall Number: Z-0761-2017

Event ID: 75743

Reason for Recall:

Customer complaint was received relating to a LifePak15 device that would power on then power down unexpectedly after a short period of use. When the LP15 powered down, power could be immediately restored by activation of the power button. The device was connected to a cellular modem from MultiTech systems for use with LIFE NET services. The corrective action was completed by Velocitor Solutions in December 2010.

Status: Terminated

Product Quantity: 1399 units (866 in the US and 533 outside US)

Code Information:

This action was taken by Velocitor Solutions to notify their customers in 2010. The consignee list was not provided to Physio-Control.

Distribution Pattern:

worldwide

Voluntary or Mandated:

Voluntary: Firm initiated