FDADecember 15, 2025device

Allura Xper FD10; Model Number: 722026;

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

00884838054189

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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