Azurion
Reported: September 13, 2023 Initiated: July 19, 2023 #Z-2403-2023
Product Description
Azurion
Reason for Recall
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
Details
- Recalling Firm
- Philips Medical Systems Nederland B.V.
- Units Affected
- 5432 systems in total
- Distribution
- US Nationwide Distribution
- Location
- Eindhoven, N/A
Frequently Asked Questions
What product was recalled? ▼
Azurion. Recalled by Philips Medical Systems Nederland B.V.. Units affected: 5432 systems in total.
Why was this product recalled? ▼
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 13, 2023. Severity: Moderate. Recall number: Z-2403-2023.
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