Philips recalls Allura Xper FD10 medical imaging systems with model 722003 where the drip tray under the cooling unit wasn't properly installed. This could lead to coolant contacting electrical parts, 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 a limited number of Allura Xper FD10 medical imaging systems (model 722003) because the drip tray under the cooling unit wasn't installed correctly. If not installed, coolant could contact electrical components, causing short circuits and system shutdowns.
In some Allura Xper FD10 systems, the drip tray beneath the cooling unit wasn't installed correctly or documented. If missing, coolant liquid could contact electrical components, leading to short circuits that might cause the system to shut down.
Medical facilities using the Allura Xper FD10 system with model number 722003 are most at risk. The issue affects systems where the drip tray wasn't properly installed or documented.
Check if your Allura Xper FD10 system has model number 722003. The recall includes specific serial numbers listed in the official notice.
Verify if the drip tray under the cooling unit is properly installed and documented.
Philips identified that in some Allura Xper FD10 systems (model 722003), the drip tray beneath the cooling unit wasn't installed correctly or documented.
Coolant liquid could contact electrical components, causing short circuits that might lead to system shutdowns.
Check if your Allura Xper FD10 has model number 722003 and if it's listed in the provided serial numbers.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1064-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1064-2026 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.
