Philips recalls Xper FD20 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch. Affected units may not start or intermittently stop X-ray imaging during use. Consumers should contact Philips for details.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips has recalled all Xper FD20 X-ray systems with specific system codes (722006, 722012, 722028) because they may not start or intermittently stop X-ray imaging when using the wired foot switch. This could lead to incomplete scans or failed imaging procedures.
The X-ray 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 examinations.
Medical facilities and healthcare professionals who use the Xper FD20 X-ray systems with the specified system codes are most at risk. Patients using these systems for imaging may experience incomplete scans or failed procedures.
Check the system code on your Xper FD20 X-ray system. Affected units have system codes 722006, 722012, or 722028. The system serial numbers are listed in the recall notice.
Identify your system code by checking the device label or documentation. Affected units have system codes 722006, 722012, or 722028.
Philips has recalled all Xper FD20 X-ray systems with system codes 722006, 722012, or 722028 due to potential failure to initiate or intermittently stop X-ray imaging when using the wired foot switch.
Check the system code on your device. Affected units have system codes 722006, 722012, or 722028. The system serial numbers are listed in the recall notice.
Contact Philips directly for further instructions. The recall does not specify a remedy, so affected users should reach out to Philips for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1663-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1663-2026 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.
