Proteus XR/a General Purpose Radiographic System
Brand(s)
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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