GE Healthcare, LLC: Medical Device Recall in 2019 - (Recall #: Z-1748-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Discovery IQ Product Usage: The systems are intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging and localization of emission activity in patient anatomy by means of integrated PET and CT images.

Product Classification:

Class II

Date Initiated: February 12, 2019

Date Posted: June 26, 2019

Recall Number: Z-1748-2019

Event ID: 82982

Reason for Recall:

GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

Status: Ongoing

Product Quantity: 1113 in total

Code Information:

Discovery IQ

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

FDA Mandated