Philips recalls Allura Xper FD10 medical imaging systems with model 722026 where the drip tray under the 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 722026) because the drip tray beneath the cooling unit wasn't installed correctly in some units. This could cause coolant to contact electrical parts, leading to short circuits and system shutdowns.
If the drip tray under the cooling unit isn't properly installed, coolant liquid might come into contact with electrical components. This could cause electrical short circuits, which may trigger system fuses and shut down the device.
Medical facilities using the Allura Xper FD10 system with model number 722026 are most at risk. Patients and staff could be affected if the system shuts down unexpectedly during procedures.
Check for the model number 722026 on the Allura Xper FD10 system. The serial numbers listed in the recall include 969, 223, 648, and other numbers.
Verify that the drip tray under the cooling unit is properly installed and documented.
Philips identified that in some units the drip tray beneath the cooling unit wasn't installed correctly or documentation wasn't adequate, which could cause coolant to contact electrical parts.
If the drip tray isn't installed, coolant liquid might contact electrical components, causing short circuits that could shut down the system.
Check for model number 722026 on the Allura Xper FD10 system. The recall lists specific serial numbers, including 969, 223, 648, and others.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1073-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1073-2026 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.
