Health product recall

Proteus XR/a General Purpose Radiographic System

Last updated

Summary

Product
Proteus XR/a General Purpose Radiographic System
Issue
Medical devices - Labelling and packaging
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Proteus XR/a General Purpose Radiographic System

More than 10 numbers, contact manufacturer.

2259973
5408826
S3918JD
S3918KD/KE
S3918LL
2259988
5399373
5399375
S3918J
S3918KF/KG
2212259
2259976
5441870)
S3918KA
2268970
2286799-12
2408033
S3918JA
S3918JB
S3918KC
2244165
S3918JC
S3918JL/JM
6124101
S3918M/MC
2259973-3

Issue

GE Healthcare has become aware that the XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices.

Recall Start Date: July 24, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Ge Hualun Medical Systems Co. Ltd.

No.1 Yong Chang North Road, Beijing, Beijing, China, 100176

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75925

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