GE Healthcare, LLC: Medical Device Recall in 2020 - (Recall #: Z-0127-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.

Product Classification:

Class II

Date Initiated: September 8, 2020

Date Posted: October 28, 2020

Recall Number: Z-0127-2021

Event ID: 86452

Reason for Recall:

Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.

Status: Terminated

Product Quantity: 30 devices total

Code Information:

Model: 5741000 and 5741000-20

Distribution Pattern:

Worldwide distribution - US Nationwide distribution including in the states of FL, KY, NC, NJ, NM, NY, TX, UT and WA. The countries of Canada, Hungary, India, Korea, China, Russia, Taiwan, Puerto Rico and Ubekistan.

Voluntary or Mandated:

Voluntary: Firm initiated