Philips recalls Allura Xper FD10 medical imaging systems with model 722010 where drip tray under cooling unit wasn't properly installed, risking electrical shorts 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 a limited number of Allura Xper FD10 medical imaging systems (model 722010) because the drip tray under the cooling unit wasn't properly installed or documented. This could cause coolant to contact electrical parts, leading to short circuits and system shutdowns.
If the drip tray beneath the cooling unit isn't properly installed or documented, coolant liquid may contact electrical components. This could cause electrical short circuits, triggering system fuses and shutting down the medical imaging system.
Healthcare facilities using the Allura Xper FD10 system with model number 722010 are most at risk. Patients and staff could face system shutdowns during procedures.
Check for the model number 722010 on the Allura Xper FD10 system. The recall affects specific serial numbers listed in the official notice.
Ensure the drip tray under 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 wasn't properly installed or documented, which could cause coolant to contact electrical components and lead to short circuits.
Check if your Allura Xper FD10 system has model number 722010 and verify the drip tray installation. If unsure, contact Philips for guidance.
The recall does not specify a fix; the remedy is null, meaning users must ensure proper installation and documentation.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1068-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1068-2026 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.
