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Uroskop omnia

Official notice

19 Jun 2025

CriticalHealth Canada

An official Health Canada notice concerns Uroskop omnia. 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 Published 2025-06-19.

What to do now

Contact the manufacturer if you require additional information.

Recall number

77632

Official notice

2025-06-19

The hazard

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

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

77632

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Affected products

Product 1

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

Risk / hazard

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

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Siemens, Uroskop Omnia.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

critical

Recall details

Recall number

77632

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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