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Health product recall

ERGO++ RTP SOFTWARE (2017-09-27)

Starting date:
September 27, 2017
Posting date:
October 6, 2017
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
Healthcare Professionals, General Public, Hospitals
Identification number:
RA-64770

Affected products

ERGO++ RTP SOFTWARE

Reason

Elekta has become aware of the potential for incorrect DICOM mapping of the exported collimator or couch angles from ERGO, which would lead to incorrect rotation of the collimator or couch when using a MLC device for planning.

Affected products

ERGO++ RTP SOFTWARE

Lot or serial number

VERSION 1.7.3 AND HIGHER

Model or catalog number

9600

Companies
Manufacturer
Elekta Business Area Software Systems Impac Medical Systems
Inc.
13723 Riverport Drive
Missouri
UNITED STATES