FDAFebruary 2, 2022device

Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Azurion (Model Numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228) running StentBoost Live (Model Number 459801781661) Software Ver...

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

The hazard

Due to a software defect, the Philips StentBoost Live R2.0 might not process X-ray images of the current run and instead show an image processed in a previous run. The image shown could be from the same patient or from a different patient.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

008848380590300088483808527500884838059054008848380853500088483808536700884838054202008848380992410088483809925800884838099272008848380852680088483809923400884838085251

Recall history

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

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