Philips recalls Zenition 50 medical devices due to wireless foot switch pedals potentially getting stuck, causing unintended radiation emissions during procedures. Affected units have specific product codes and were sold for diagnostic imaging.
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 its Zenition 50 medical imaging devices because a wireless foot switch pedal can get stuck after release, leading to unintended radiation emissions. This could pose a risk during medical procedures, especially for patients.
The wireless foot switch pedal can get stuck in the active position when released, causing the device to emit unintended radiation. This could happen during medical procedures, potentially exposing patients or staff to unnecessary radiation.
Healthcare professionals using the Zenition 50 devices for medical imaging procedures are most at risk. Patients undergoing these procedures may also be affected if the device malfunctions.
Check for product codes 718096, 459801442981, 459801238231, 459801257861, 459800627394, 459800415535, or 459800415542 on the device. The Zenition 50 devices are used for medical imaging procedures on patients (except neonates).
Look for product codes listed in the recall notice to confirm if your device is affected.
Reach out to Philips customer service for guidance on next steps if your device is affected.
No, the devices are not intended for use on neonates (birth to one month).
Contact Philips customer service for specific instructions on how to handle the device.
The recall notice does not specify repair options; contact Philips for details.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1580-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1580-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
