ClearanceBrief
Recall Z-0974-2024 ยท LNH System, Nuclear Magnetic Resonance Imaging

Philips North America

Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system

DateFeb 2, 2024 (initiated Jan 6, 2022)
StatusOpen, Classified
ReasonMagnetic materials were used for the wheels of trolley. Wheels with magnetic material might be attracted to MRI systems if the wheels are in the magnetic field.
Root causeDevice Design
ActionBeginning in January 2022, Philips Field Service Engineers (FSE) visited impacted customer sites to replace the magnetic castor wheels of the HA Flextrack Trolley II with non-magnetic castor wheels. All reachable systems were addressed as of August 10, 2023.
Quantity2
DistributionWorldwide - US Nationwide distribution in the states of FL and NY. The countries of Denmark, Norway, and Sweden.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K173356Ingenia Elition S and Ingenia Elition X R5.4
Philips Medical Systems Nederland B.V., Mar 6, 2018
K173451Ingenia Elition S and Ingenia Elition X
Philips Medical Systems Nederland B.V., Mar 20, 2018