Product Safety Recalls

Product Recall Tracker

GE Healthcare, LLC Recall 87023

Description: GE NM/CT 870 CZT system Model Number H3906CW - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body.

GE Healthcare, LLC Recall 87023 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0855-2021
Event ID87023
Event DescriptionGE NM/CT 870 CZT system Model Number H3906CW - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body.
Product TypeDevices
DistributionWorldwide
Quantity12 units
Recall ReasonGE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.
Device Classification20210120
Device Code InfoSerial numbers: 87CY63028, 87CZ63044, 87CZ63045, 87CZ63042, 87CY63025, 87CY63029, 87CY63027, 87CY63030, 87CZ63046, 87CY63034, 87CY63032, 87CY63033
Center Classification Date20210113
Recall Initiation Date20201210
Recalling FirmGE Healthcare, LLC
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.