FDAJanuary 2, 2024device

Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: Imaging Processing PC, Host PC, FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10 OR Table 722...

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

The hazard

Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

008848380590300088483805919100884838054189008848380808050088483805419600884838059115008848380590540088483805920700884838054202008848380592690088483805906100884838059085

Recall history

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

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