RADREX-i (2017-12-19)

Starting date:

December 19, 2017

Posting date:

January 29, 2018

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-65742

• 
  Reason
• 
  Affected products

Affected products

RADREX-i

Reason

In an occurrence, it has been found that when an operator performed an exam with the wireless x-ray detector, an error message dialog was displayed on the console. After a system reboot, the image data was lost.

Affected products