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Official recall record

Uroskop Omnia

Health Canada — Medical Devices · 2025-06-19 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-06-19
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

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

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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