Philips recalls Allura Xper FD10/10 systems with model 722027 where drip tray under cooling unit wasn't installed. This could cause electrical shorts and system shutdowns. Affected units may need repair.
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 Allura Xper FD10/10 systems with model number 722027. The recall is because the drip tray under the cooling unit might not have been installed correctly, which could cause electrical shorts and system shutdowns.
If the drip tray under the cooling unit isn't installed correctly, coolant liquid could contact electrical components. This might cause electrical short-circuits, leading to system shutdowns.
Medical professionals using the Allura Xper FD10/10 systems with model number 722027 are most at risk. The recall affects a limited number of units where the drip tray installation was not properly documented.
Check for model number 722027 on the Allura Xper FD10/10 system. The recall includes specific serial numbers listed in the official notice.
Ensure the drip tray beneath the cooling unit is properly installed and documented.
Philips identified that in some units the drip tray under the cooling unit wasn't installed correctly or documented, which could cause electrical shorts and system shutdowns.
Model number 722027 for Allura Xper FD10/10 systems.
No, but you should check if the drip tray is properly installed and documented to avoid potential electrical issues.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1074-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1074-2026 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.
