Philips recalls Ingenia Elition X patient transport trolley with magnetic wheels that could be attracted to MRI machines, posing a risk during scans. Affected units have specific serial numbers and were sold in the U.S. between 2019 and 2022.
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 trolleys that have magnetic wheels. These wheels could be pulled toward MRI machines, potentially causing injury during scans. The recall affects specific models sold in the U.S. from 2019 to 2022.
The trolley's wheels contain magnetic materials that could be attracted to the strong magnetic fields used in MRI machines. If the trolley is near an MRI machine during a scan, the wheels might move unexpectedly, causing injury to the patient or staff.
Healthcare workers using the trolley in MRI facilities and patients undergoing scans are most at risk. The recall applies to specific models sold in the U.S. between 2019 and 2022.
Check for the product number 781358 and accessory number 989710008732 on the trolley. The recall applies to units sold in the U.S. from 2019 to 2022 with specific serial numbers.
Inspect the trolley wheels for magnetic materials that could be attracted to MRI machines.
Reach out to Philips North America for specific serial numbers and next steps.
The trolley's wheels contain magnetic materials that could be attracted to MRI machines, posing a risk during scans.
Check for product number 781358 and accessory number 989710008732 on the trolley. The recall applies to units sold in the U.S. from 2019 to 2022.
Contact Philips North America for specific serial numbers and next steps. The recall does not include a fix or replacement.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0974-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0974-2024 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.
