Philips recalls Allura Xper FD20/10 X-ray systems with system code 722029 due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips is recalling all Allura Xper FD20/10 X-ray systems with system code 722029 because the X-ray imaging may not start or may stop unexpectedly when using the wired foot switch. This could lead to incomplete scans or repeated imaging attempts, which might affect patient safety and diagnostic accuracy.
The X-ray imaging may not start or may stop intermittently when using the wired foot switch. This could cause incomplete scans or repeated imaging attempts, potentially affecting patient safety and diagnostic accuracy.
Healthcare facilities using Philips Allura Xper FD20/10 X-ray systems with system code 722029 are most at risk. Patients and staff during imaging procedures could be affected if the system fails to initiate X-rays properly.
Check for system code 722029 on the device. The system code is listed in the product description and can be found on the device's label or documentation.
Verify the system code on the device label or documentation to confirm if it matches 722029.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Check the system code on the device label or documentation. If it matches 722029, contact Philips for further instructions.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1668-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1668-2026 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.
