Philips recalls specific Allura Xper Interventional Fluoroscopy systems where the Disk Bay may not function properly, potentially delaying medical procedures. Affected models include Allura Xper FD10, FD10C, FD10/10, FD10/15, FD10/20, FD20, FD20 Biplane, and FD20/10, FD20/15, FD20/20 systems with specific serial numbers.
Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.
Philips is recalling certain Allura Xper Interventional Fluoroscopy systems due to a potential issue with the Disk Bay component that may cause the system to stop functioning and delay medical procedures. This affects specific models and serial numbers.
The Disk Bay component may not perform as intended, leading to the system stopping functionality and preventing imaging during procedures. This could delay critical medical treatments, but does not pose an immediate risk of injury to users.
Medical facilities that own or use the affected Philips Allura Xper Interventional Fluoroscopy systems are most at risk. The recall impacts specific models and serial numbers used in hospitals and clinics.
Check if your system is listed in the affected models: Allura Xper FD10, FD10C, FD10/10, FD10/15, FD10/20, FD20, FD20 Biplane, or FD20/10, FD20/15, FD20/20. Verify the specific serial numbers provided in the recall notice.
Identify your Philips Allura Xper Interventional Fluoroscopy system model to see if it matches the affected models listed in the recall.
Confirm if your system has the specific serial numbers listed in the recall notice for the affected models.
Affected models include Allura Xper FD10, FD10C, FD10/10, FD10/15, FD10/20, FD20, FD20 Biplane, and FD20/10, FD20/15, FD20/20 systems with specific serial numbers listed in the recall notice.
No action is required if your system model and serial numbers do not match the affected models and serial numbers listed in the recall notice.
The recall notice does not specify a fix or remedy for this issue.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1151-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1151-2024 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.
