UROSKOP Omnia Max. Model Number: 10762473
Reported: June 25, 2025 Initiated: June 4, 2025 #Z-1982-2025
Product Description
UROSKOP Omnia Max. Model Number: 10762473
Reason for Recall
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 25 units
- Distribution
- Nationwide distribution.
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
UROSKOP Omnia Max. Model Number: 10762473. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 25 units.
Why was this product recalled? ▼
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 25, 2025. Severity: Moderate. Recall number: Z-1982-2025.
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