FDAFebruary 3, 2015device

Philips Healthcare INTEGRIS H5000F/Allura 9F Model : 722017 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and thrombolysis and athere...

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

The hazard

Monitor Ceiling Suspension system may fall

What to do

FDA enforcement status: Terminated

Brands named

philips medical systemsphilipsphilips medical

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 →