Philips recalls Allura Xper FD10F medical systems with model 722002 due to potential coolant contact with electrical components causing short circuits and system shutdowns.
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
Philips is recalling all Allura Xper FD10F medical systems with model number 722002 because the drip tray under the cooling unit may not be properly installed. This could cause coolant to contact electrical parts, leading to short circuits and system shutdowns.
If the drip tray beneath the cooling unit is not installed correctly, coolant liquid may come into contact with electrical components. This can cause electrical short circuits, which might trigger system fuses and shut down the medical device.
Medical facilities using the Allura Xper FD10F system with model number 722002 are most at risk. This recall affects systems that were not properly corrected or documented for the drip tray installation.
Check for the model number 722002 on the Allura Xper FD10F system. This recall applies to systems that were not properly corrected or documented for the drip tray installation.
Verify that the drip tray beneath the cooling unit is properly installed and documented as per field corrections.
Philips identified that in some systems the drip tray beneath the cooling unit was not installed correctly or documentation of the installation was inadequate, which could lead to coolant contacting electrical parts.
If the drip tray is not installed, coolant liquid may contact electrical components, causing short circuits that could trigger system fuses and shut down the medical device.
Check for the model number 722002 on your Allura Xper FD10F system. This recall applies to systems that were not properly corrected or documented for the drip tray installation.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1063-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1063-2026 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.
