Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:16008
Brand Name:GE PET Discovery 600 and Discovery 690 Nuclear Medicine System
Model:600 & 690
Affected:
Software version:Software versions pet_mict_plus.44 and pet_velocity.53
Recalling Organisation:GE Healthcare Limited
Level 7, Vero Centre
48 Shortland St
Auckland 1010
Contact Information:0800 659 465
Manufacturer:GE Medical Systems LLC
Issue:A software issue exists when using List Mode Replay, such that subsequent reconstructions with that data could contribute to an image with scatter over-estimation and overcorrection. Reconstructed images with this issue will have many fewer counts than the acquired scan data and a high scatter fraction.
This issue may affect studies that use List Mode Replay and are reconstructed after subsequent acquisitions.
This issue may lead to image misinterpretation and/or inaccurate treatment decisions
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:9/1/2014
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