Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.
Reported: April 30, 2025 Initiated: February 25, 2025 #Z-1582-2025
Product Description
Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.
Reason for Recall
A wireless 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 North America Llc
- Units Affected
- N/A
- Distribution
- US
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.. Recalled by Philips North America Llc. Units affected: N/A.
Why was this product recalled? ▼
A wireless 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 April 30, 2025. Severity: Moderate. Recall number: Z-1582-2025.
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