FDAAugust 8, 2024device

Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional Fluoroscopic X-Ray System, Model Numbers 722010, 722012, 722013

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

The hazard

A half-threaded bolt was included in the LTE kits instead of the correct full-threaded bolt.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

Recall history

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

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