Philips recalls Ingenia 3.0T MRI systems with potentially incorrectly installed patient support table floor plates. This could affect safety during medical procedures. Check your model numbers and serial numbers for affected units.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Ingenia 3.0T MRI systems because the patient support table floor plate may be incorrectly installed. This could lead to safety risks during medical procedures if the table is not properly secured.
The patient support table floor plate may be incorrectly installed, which could cause the table to become unstable during MRI procedures. This instability might lead to the table shifting or moving unexpectedly, potentially causing injury to the patient or staff.
Medical facilities that own or use Philips Ingenia 3.0T MRI systems with model numbers 781377, 781342, or 782103 are most at risk. Patients using these systems during procedures may face safety issues if the table is not correctly installed.
Check your Philips Ingenia 3.0T MRI system's model numbers (781377, 781342, 782103) and serial numbers listed in the recall notice. The recall includes specific serial numbers and UDI-DI codes provided in the official notice.
Verify that the patient support table floor plate is installed correctly according to Philips' guidelines.
Model numbers 781377, 781342, and 782103 are affected.
Check your model numbers and serial numbers against the list provided in the recall notice.
No, but you should check the installation of the patient support table floor plate to ensure it is correctly installed.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1566-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1566-2024 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.
