AllClear
PricingSign in
FDAMarch 3, 2026device

ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;

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

The hazard

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

0088483805907800884838054233

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →