Philips recalls Ingenia Ambition X patient transport systems with HA FlexTrak II accessory due to potential MRI safety risks from magnetic wheels. Affected units may be attracted to MRI machines if in the magnetic field.
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.
Philips is recalling patient transport systems that include magnetic wheels which could be attracted to MRI machines. This poses a risk of injury if the transport is used near an MRI scanner.
The wheels contain magnetic materials that might be pulled toward MRI machines if the transport is placed in the magnetic field. This could cause the transport to move unexpectedly, potentially injuring patients or staff.
Healthcare facilities using Philips Ingenia Ambition X patient transport systems with HA FlexTrak II accessory are most at risk. Patients and staff using these systems near MRI equipment could face injury.
Check for the product number 781356 on the Ingenia Ambition X system and accessory number 989710008732 on the HA FlexTrak II. The recall covers specific serial numbers listed in the UDI-DI code.
Verify the product number 781356 and accessory number 989710008732 on your system.
The wheels contain magnetic materials that could be attracted to MRI systems if the transport is in the magnetic field, posing a risk of injury.
Check for product number 781356 on the Ingenia Ambition X system and accessory number 989710008732 on the HA FlexTrak II. The recall covers specific serial numbers listed in the UDI-DI code.
The recall does not specify a remedy, so contact Philips directly for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0975-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0975-2024 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
