Health product recall

Proteus XR/a General Purpose Radiographic System (2019-08-09)

Starting date:
August 9, 2019
Posting date:
August 30, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-70843

Last updated: 2019-09-05

Affected Products

Proteus XR/a General Purpose Radiographic System

Reason

GE Healthcare has become aware that when using the Proteus XR/a radiographic system, the user may not hear the tone for short exposures. This issue could result in an incorrect radiation exposure indication display/output.

Affected products

Proteus XR/a General Purpose Radiographic System

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

5441870

Companies
Manufacturer

GE Hualun Medical Systems Co. Ltd.

No.1 Yong Chang North Road,, Beijing Economic Technological, Development Zone,

Beijing

100176

CHINA