Philips recalls ALLURA Xper FD20 OR Table systems with specific system codes due to potential failure in initiating X-ray imaging when using the wired foot switch. Affected units may require repair or replacement.
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 OR Table systems with specific system codes because the X-ray imaging may not start or could work intermittently when using the wired foot switch. This could lead to incomplete or inconsistent imaging during procedures.
The wired foot switch may fail to initiate X-ray imaging properly or work inconsistently, leading to incomplete or inconsistent imaging during medical procedures. This could result in missed diagnoses or the need for repeat scans.
Medical facilities using the ALLURA Xper FD20 OR Table systems with system codes 722015, 722023, or 722035 are most at risk. Patients undergoing imaging procedures may experience incomplete scans due to the issue.
Check the system code on the device: 722015, 722023, or 722035. The system serial numbers are listed in the recall notice for each code.
Identify the system code on your device (722015, 722023, or 722035) to determine if it is affected.
Reach out to Philips for guidance on next steps, as the recall remedy is not specified in the record.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
The recall remedy is not specified in the official notice. Contact Philips directly for instructions.
Yes, system codes 722015, 722023, and 722035 are affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1665-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1665-2026 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.
