FDAMay 3, 2024device

HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710006412

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

The hazard

Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838099470989710006412

Recall history

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

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