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U.S. Department of Health and Human Services

Class 2 Device Recall Ingenia Ambition X

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 Class 2 Device Recall Ingenia Ambition Xsee related information
Date Initiated by FirmJanuary 06, 2022
Date PostedFebruary 02, 2024
Recall Status1 Open3, Classified
Recall NumberZ-0975-2024
Recall Event ID 93737
510(K)NumberK181479 K183063 K193215 
Product Classification System, nuclear magnetic resonance imaging - Product Code LNH
ProductIngenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
Code Information UDI-DI 00884838090040 Ingenia Serial number / Accessory Serial Number 47004 100020 47019 100024 47190 100022 47200 100025 47210 100019 47227 100063 47231 100056 47271 100032 47281 100028 47281 100031
Recalling Firm/
Manufacturer		 Philips North America
222 Jacobs St
Cambridge MA 02141-2296
For Additional Information ContactCustomer Care Solution Center
800-722-9377
Manufacturer Reason
for Recall		Magnetic 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.
FDA Determined
Cause 2		Device 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.
Quantity in Commerce10
DistributionWorldwide - US Nationwide distribution in the states of FL and NY. The countries of Denmark, Norway, and Sweden.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database510(K)s with Product Code = LNH
510(K)s with Product Code = LNH
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