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Health product recall

Compass 3.0 (2013-08-19)

Starting date:
August 19, 2013
Posting date:
June 5, 2014
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-39809

Recalled Products

Compass 3.0

Reason

Under certain conditions, resampling of regions of interest (ROI) geometries to the dose grid representation is not correctly calculated and an additional voxel layer is added incorrectly on the superior side of each ROI.

Affected products

Compass 3.0

Lot or serial number

Not applicable

Model or catalog number

CS10-100

Companies
Manufacturer
IBA Dosimetry GmbH
Bahnhofstrasse 5
Schwarzenbruck
90592
GERMANY