Philips recalls limited Allura Xper FD10C systems with model 722001 where drip tray under cooling unit wasn't properly installed. This could cause electrical shorts, system shutdowns, and potential safety risks.
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 a limited number of Allura Xper FD10C medical systems with model number 722001. The recall is because the drip tray under the cooling unit wasn't installed correctly in some units, which could lead to 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 and potential safety risks.
Medical facilities using the Allura Xper FD10C system with model number 722001 are most at risk. This recall affects specific units that were not properly corrected during installation.
Check for model number 722001 on the Allura Xper FD10C system. The recall includes specific serial numbers listed in the official notice.
Verify if the drip tray under the cooling unit was installed correctly according to field corrections.
Philips identified that in some units the drip tray under the cooling unit wasn't installed properly or documentation wasn't adequate, which could cause electrical shorts.
Model number 722001 for the Allura Xper FD10C system.
No, but you should check if the drip tray was installed correctly to prevent 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-1062-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1062-2026 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.
