Philips recalls ALLURA Xper FD20 Biplane or Table systems with specific serial numbers due to potential X-ray imaging failures when using the wired foot switch. Affected units may not initiate or intermittently produce X-rays, posing a risk of improper imaging during procedures.
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 ALLURA Xper FD20 Biplane or Table systems with specific serial numbers because the wired foot switch may cause X-ray imaging to not start or work intermittently. This could lead to improper medical imaging during procedures, potentially affecting patient safety.
The wired foot switch may fail to initiate X-ray imaging or cause it to work intermittently. This could result in improper imaging during medical procedures, potentially leading to incorrect diagnoses or treatment decisions.
Medical facilities using the ALLURA Xper FD20 Biplane or Table systems with System Codes 722020 or 722025 are most at risk. Patients undergoing imaging procedures with these systems could be affected if the X-ray imaging fails to start or works intermittently.
Check for System Code 722020 or 722025 on the device. System Code 722020 has a Serial Number 4, and System Code 722025 has Serial Numbers 6, 2, or 3.
Identify the System Code on the device to determine if it is 722020 or 722025.
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. If it is 722020 or 722025, 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-1666-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1666-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
