Philips recalls Allura Xper medical imaging systems with specific model numbers due to hand switch button not fully releasing, potentially causing loss of imaging or unintended radiation exposure.
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
Philips is recalling Allura Xper medical imaging systems with specific model numbers because the hand switch button may not fully release, leading to loss of imaging functionality or unintended radiation exposure. This could affect medical procedures and patient safety.
The hand switch button on these systems may not fully release, which can cause the imaging process to stop unexpectedly or lead to unintended radiation exposure and additional contrast injections. This could disrupt medical procedures and pose risks to patients.
Medical facilities using Philips Allura Xper systems with the listed model numbers are most at risk. Patients undergoing imaging procedures may be affected if the system malfunctions.
Check the model number on your Philips Allura Xper system. The affected models include specific FD10C, FD10F, FD10, FD20, and other variants with model numbers starting with 722001 through 722059.
Identify the model number on your Philips Allura Xper system to determine if it is affected by this recall.
Reach out to Philips customer support for guidance on next steps if your model is listed in the recall.
The affected model numbers include 722001 for Allura Xper FD10C, 722002 for Allura Xper FD10F, and other specific variants listed in the recall notice.
The hand switch button may not fully release, which could cause loss of imaging functionality or unintended radiation exposure and additional contrast injections.
No, the recall does not require immediate discontinuation. Medical facilities should check the model number and contact 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-2412-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2412-2026 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.
