Health product recall

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

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

MOBILETT Elara Max

Lot or serial number

10059

Model or catalog number

11107444

Companies
Manufacturer
Siemens Healthcare GmbH
Henkestr. 127
Erlangen
91052
GERMANY