Health product recall

Uroskop Omnia

Last updated

Summary

Product
Uroskop Omnia
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Affected products

Affected products Lot or serial number Model or catalog number
Uroskop Omnia More than 10 numbers, contact manufacturer. 10094910

Issue

During internal pro-active quality assurance, an issue with the resistor in the frequency converter was discovered. The problem can occur under very rare circumstances due to an undetectable defect in the frequency inverter for the longitudinal table movement (defective relay) and when this movement is activated in frequent succession at the same time. This may lead to overheating of a resistor in the frequency converter. If, in addition to several installation-related factors coincide unfavorably, it cannot be ruled out that the plastic housing will catch fire. The root cause of the issue is an undetectable defect in the frequency inverter and unfavorable
installation-related factors.

Recall start date: June 17, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Siemens Healthcare GmbH

Henkestr. 127, Erlangen, Germany, 91052

Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-77632

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