Philips recalls Zenition 70 medical devices due to wireless foot switch potentially getting stuck, causing unintended radiation emissions during procedures. Affected units have specific product codes and serial numbers.
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 70 medical imaging devices because a wireless foot switch pedal can get stuck after release, leading to unintended radiation exposure. This could pose a risk during medical procedures, especially for patients.
The wireless foot switch pedal can become stuck in the active position when released, causing the device to emit unintended radiation. This could happen during medical procedures, potentially exposing patients to unnecessary radiation.
Healthcare providers using the Zenition 70 devices for medical procedures are most at risk. Patients undergoing procedures with these devices may also be affected if the radiation emission occurs.
Check for the product code 718133 on the Zenition 70 device. The affected units include specific wireless foot switch sets and base stations with listed serial numbers.
Verify if the wireless foot switch pedal gets stuck when released by testing the device.
The recalled Zenition 70 devices have product code 718133 and specific serial numbers listed in the recall notice.
Yes, the unintended radiation emission could expose patients to unnecessary radiation during procedures.
Check for product code 718133 and the listed serial numbers for wireless foot switch sets and base stations.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1581-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1581-2025 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.
