Physio-Control, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1257-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.

Product Classification:

Class I

Date Initiated: January 13, 2017

Date Posted: March 15, 2017

Recall Number: Z-1257-2017

Event ID: 76252

Reason for Recall:

The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage.

Status: Terminated

Product Quantity: total 133,330 units (50,046 units in the US)

Code Information:

Affected Product Part Numbers: 320371500XX. There are 133,330 affected serial numbers.

Distribution Pattern:

Worldwide Distribution - US (nationwide) and in the following countries: Bahrain, Belize, Cambodia, Chile, China, C¿te d'Ivoire, Ecuador, Germany, Honduras, Hong Kong, India, Indonesia, Jamaica, Myanmar, Netherlands, Niger, Philippines, Saudi Arabia, Senegal, Singapore, Sri Lanka, Thailand, Tunisia, Ukraine, and Zambia.

Voluntary or Mandated:

Voluntary: Firm initiated