Philips recalls Allura Xper FD20/10 systems with model 722029 where drip tray 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 Allura Xper FD20/10 medical imaging systems with model number 722029. The recall happens because the drip tray under the cooling unit might not be installed correctly, which could cause coolant to contact electrical parts and lead to system shutdowns.
If the drip tray isn't installed correctly, coolant liquid could contact electrical components. This might cause electrical short-circuits, leading to system shutdowns and potential interruptions in medical imaging services.
Medical facilities using Philips Allura Xper FD20/10 systems with model number 722029 are affected. Staff handling these systems are most at risk if the drip tray isn't installed properly.
Check for model number 722029 on the Allura Xper FD20/10 system. The recall applies to systems with serial numbers 30, 81, 80, or 47.
Verify that the drip tray beneath the cooling unit is properly installed and documented.
Philips identified that in some systems the drip tray wasn't installed correctly or documentation wasn't adequate, risking electrical shorts.
Coolant liquid might contact electrical components, causing short circuits that could shut down the system.
Check for model number 722029 with serial numbers 30, 81, 80, or 47.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1076-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1076-2026 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.
