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Health product recall

Omnipro-Accept (2013-08-07)

Starting date:
August 7, 2013
Posting date:
January 6, 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-37261

Recalled products

  1. Omnipro-Accept 

Reason

Malfunction in software Omnipro-Accept version 7.4A which may potentially lead to inappropriate data transfer to treament planning systems (Software error in resampling function).

Affected products

A. Omnipro-Accept

Lot or serial number

Not applicable

Model or catalog number
  • 997-105
Companies
Manufacturer
Iba Dosimetry GmbH
Bahnhofstrasse 5
Schwarzenbruck
90592
GERMANY