Philips recalls Ingenia Elition X MRI systems with potentially incorrectly installed patient support table floor plates. Affected models include specific serial numbers and UDI-DI codes. No remedy is listed in the recall notice.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Ingenia Elition X MRI systems because the patient support table floor plate might be installed incorrectly. This could lead to safety issues during medical procedures if the table isn't properly secured.
The patient support table floor plate may be incorrectly installed, which could cause the table to become unstable during medical procedures. This might lead to patient injury if the table shifts unexpectedly while a patient is being scanned.
Healthcare facilities that own or use the recalled Ingenia Elition X MRI systems are most at risk. Patients using these systems are not directly affected by the issue.
Check if your MRI system has a model number of 782136, 781358, 78217, or 782119. Look for specific serial numbers listed in the recall notice, including UDI-DI codes 884838108622, 884838098336, etc.
Verify your MRI system's model number and serial numbers against the list provided in the recall notice.
The recall addresses potential instability of the patient support table floor plate during medical procedures. Patients are not directly affected by the issue, but healthcare facilities must ensure the system is safe before use.
No remedy is listed in the recall notice, so there is no immediate action required to stop using the system. Healthcare facilities should check the product details to confirm if their system is affected.
Check your model number (782136, 781358, 78217, or 782119) and serial numbers against the list provided in the recall notice, including UDI-DI codes.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1571-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1571-2024 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.
