FDAJune 12, 2023device

Azurion 7 M20. X-ray Image guided Therapy System.

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

The hazard

The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

0088483808526800884838099258

Recall history

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

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