Philips recalls 15+ models of Allura Xper fluoroscopy systems due to potential loss of imaging functionality, motorized movement, or data from unauthorized hard drives. Affected units have specific model numbers listed in the recall.
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Philips is recalling 15 different models of Allura Xper fluoroscopy systems because unauthorized hard drives could cause imaging to stop working, movement to fail, or data to be lost. This affects medical imaging equipment used in hospitals and clinics.
The recall is for potential loss of imaging functionality, motorized movement, or data from unauthorized hard drives. This is a low-risk issue as it does not involve immediate safety hazards but could affect medical imaging operations.
Medical facilities that own or use Philips Allura Xper fluoroscopy systems are most affected. This recall impacts specific model numbers listed in the recall notice, primarily used in hospital settings for medical imaging procedures.
Check if your Philips Allura Xper system has one of the 15+ model numbers listed in the recall. The recall includes specific UDI numbers and model numbers that are detailed in the recall notice.
Check the model number on your Philips Allura Xper system. The recall lists specific model numbers (e.g., 722005, 722011, etc.) that are affected.
Reach out to Philips customer support with your model number to confirm if your system is affected and get instructions on next steps.
Philips identified that unauthorized hard drives could cause imaging to stop working, movement to fail, or data to be lost. This is a low-risk issue that affects medical imaging equipment.
Check if your system has one of the specific model numbers listed in the recall notice (e.g., 722005, 722011, etc.). The recall includes detailed UDI numbers for each model.
Contact Philips customer support with your model number to get instructions on how to address the issue. They may provide guidance on removing unauthorized hard drives or other steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2891-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2891-2026 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.
