Philips recalls limited Allura Xper FD20 systems (model 722006) where drip tray under cooling unit wasn't properly installed, risking coolant contact with electrical parts and system shutdown.
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 FD20 medical systems (model 722006) because the drip tray beneath the cooling unit wasn't installed correctly in some units. This could cause coolant to contact electrical components, potentially leading to system shutdowns.
If the drip tray under the cooling unit isn't installed correctly, coolant liquid could come into contact with electrical components. This might cause electrical short circuits, which could trigger system fuses and shut down the medical device.
Medical facility staff and users of the Allura Xper FD20 system who own or use the specific model numbers listed in the recall. Those with the drip tray not properly installed are at risk of system shutdowns.
Check for the model number 722006 on the Allura Xper FD20 system. The recall includes specific serial numbers listed in the official notice. This device is used in medical facilities for imaging.
Ensure the drip tray beneath the cooling unit is properly installed and documented as part of the field correction.
Philips identified that in some Allura Xper FD20 systems (model 722006), the drip tray under the cooling unit wasn't installed correctly or documented, which could cause coolant to contact electrical components.
If the drip tray isn't properly installed, coolant liquid might contact electrical components, causing electrical short circuits that could trigger system fuses and shut down the medical device.
Check if your Allura Xper FD20 system has model number 722006 and one of the specific serial numbers listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1066-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1066-2026 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.
