Recall Monitor
Health Products

Uroskop Omnia

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - Radiology
Product: Uroskop Omnia
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: General public, Healthcare, Industry
Recall class: Type II
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Products

Affected productsLot or serial numberModel or catalog number
Uroskop OmniaMore 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

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