Philips recalls specific Allura Xper Interventional Fluoroscopic X-ray Systems with DIMMs that may stop functioning, causing procedure delays. Affected models include Allura Xper FD10, FD10/10, FD10C, FD20, and FD20/20 series with listed serial numbers.
Dual In-Line Memory Modules (DIMMs) 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 Fluoroscopic X-ray Systems because the Dual In-line Memory Modules (DIMMs) may not work properly, which can cause imaging to stop and delay medical procedures. This affects specific models with particular serial numbers.
The DIMMs (Dual In-line Memory Modules) used in these systems may not function as intended, leading to system failures and interruptions in imaging. This can delay medical procedures but does not pose a risk of injury or death.
Healthcare professionals using Philips Allura Xper Interventional Fluoroscopic X-ray Systems with the listed models and serial numbers are affected. The risk is low as the issue only causes potential delays, not immediate safety hazards.
Check if your system is an Allura Xper model with the specific model numbers listed (e.g., FD10, FD10/10, FD10C, FD20, FD20/20) and the corresponding serial numbers provided in the recall notice.
Identify your system model from the list of affected Allura Xper models (e.g., FD10, FD10/10, FD10C, FD20, FD20/20) and verify the serial numbers provided in the recall.
The DIMMs (Dual In-line Memory Modules) in these systems may not perform as intended, which can cause the system to stop functioning and delay medical procedures.
Check if your system model matches the affected Allura Xper models (FD10, FD10/10, FD10C, FD20, FD20/20) and has the specific serial numbers listed in the recall notice.
The recall does not require immediate action, but you should check your system model and serial numbers to confirm if it is affected.
We’ve drafted a message you can send PHILIPS to request your refund or repair — edit it as you like.
Subject: Recall Z-1156-2024 — PHILIPS PHILIPS Hello, I own a PHILIPS that is covered by recall Z-1156-2024 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.
