Philips recalls Veradius Unity devices due to wireless foot switch pedal getting stuck, causing unintended radiation emissions during medical procedures. Affected units have specific product codes and were sold for radiological guidance.
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.
Philips is recalling Veradius Unity medical devices because a wireless foot switch pedal can get stuck after release, leading to unintended radiation emissions during procedures. This could expose patients to unnecessary radiation if the device is used without proper control.
The wireless foot switch pedal can become stuck in the active position when released, causing the device to emit radiation without the user's intent. This unintended radiation could expose patients to unnecessary radiation during medical procedures.
Healthcare professionals using Veradius Unity devices for radiological procedures are most at risk. Patients undergoing procedures with these devices may be exposed to unintended radiation if the foot switch gets stuck.
Check for product code 718132 on the Veradius Unity device. The affected units were sold for radiological guidance procedures and include specific wireless foot switch components with model numbers listed in the recall notice.
Verify if the wireless foot switch pedal gets stuck when released by testing the device's response.
Reach out to Philips customer support for guidance on whether your device is affected and next steps.
No, the devices are not intended for use on neonates (birth to one month).
The device emits unintended radiation, which could expose patients to unnecessary radiation during procedures.
Check for product code 718132 or the specific wireless foot switch components listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1582-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1582-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
