Philips recalls specific models of interventional fluoroscopic X-ray systems (model 722400) due to unauthorized hard drives causing potential loss of imaging, movement, or data. Affected units have unique UDI numbers listed in the recall notice.
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Philips is recalling certain interventional fluoroscopic X-ray systems (model 722400) because unauthorized hard drives can cause imaging functionality to fail, loss of motorized movement, or data loss. This affects medical equipment used in procedures requiring real-time imaging.
Unauthorized hard drives installed in these X-ray systems can cause the imaging functionality to stop working, motorized movement to fail, or data to be lost. This could impact medical procedures requiring real-time imaging.
Healthcare professionals using Philips Allura Cardio Vascular-Allura Centron X-ray systems with model number 722400 are most at risk. The recall applies to specific units identified by unique UDI numbers.
Check if your Philips Allura Cardio Vascular-Allura Centron X-ray system has model number 722400. Affected units have unique UDI numbers listed in the recall notice, which include many specific combinations starting with (01)00884838042315(21).
Verify your X-ray system's model number is 722400.
Check if your unit's UDI number matches any listed combinations starting with (01)00884838042315(21).
Unauthorized hard drives in these X-ray systems can cause imaging functionality to fail, loss of motorized movement, or data loss.
Check if your model number is 722400 and your UDI number starts with (01)00884838042315(21).
No action is needed if your model number and UDI number do not match the affected units.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2893-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2893-2026 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.
