MOBILETT Elara Max (2019-06-26)

Starting date:

June 26, 2019

Posting date:

July 19, 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-70443

Last updated: 2019-07-19

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  Reason
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  Affected products

Affected Products

MOBILETT Elara Max

Reason

Siemens is providing a firmware change of the Central Processing Unit (CPU) board to improve internal communication for the MOBILETT Elara Max system. The firmware change will prevent sporadic issues with images taken outside the detector window being partially blank or black.

Affected products