Philips recalls ALLURA Xper FD20 Biplane systems with specific system codes 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 Biplane X-ray systems with system codes 722008 and 722013 because they may not start X-ray imaging properly when using the wired foot switch. This could lead to incomplete scans or failed imaging procedures during medical use.
The X-ray imaging system may fail to initiate or intermittently stop X-ray imaging when the wired foot switch is used. This could result in incomplete scans or failed imaging procedures during medical treatments.
Healthcare professionals using the ALLURA Xper FD20 Biplane X-ray systems with system codes 722008 or 722013 are most at risk. Patients undergoing X-ray procedures with these systems may experience incomplete imaging.
Check for system codes 722008 or 722013 on the device. These codes are listed in the system serial numbers provided in the recall notice.
Identify if your system has code 722008 or 722013 by reviewing the system serial numbers listed in the recall notice.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Check for system codes 722008 or 722013 on the device, as these are the specific codes listed in the recall notice.
The recall notice does not specify a remedy, so contact Philips directly for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1664-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1664-2026 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.
