Philips recalls Ingenia Elition S MRI systems with potentially incorrectly installed patient support table floor plates. This could lead to safety issues during medical procedures. Affected units have specific model and serial numbers listed in the recall.
Patient support table floor plate may be incorrectly installed.
Philips is recalling Ingenia Elition S MRI systems because the patient support table floor plate might be installed incorrectly. This could cause safety issues during medical procedures if the table isn't properly secured.
The patient support table floor plate may be incorrectly installed, which could lead to the table becoming unstable during MRI scans. This instability might cause the table to shift or move unexpectedly, potentially causing injury to the patient or staff.
Healthcare facilities that own or use the Ingenia Elition S MRI systems are most at risk. Patients undergoing MRI scans could be affected if the table isn't properly installed.
Check for model numbers 781357 or 782106 on the MRI system. Serial numbers listed in the recall include many numbers starting with 46000 through 46289. The recall covers specific units sold in the U.S. by Philips.
Verify that the patient support table floor plate is installed correctly according to the manufacturer's instructions.
Model numbers 781357 and 782106 are affected.
Check for model numbers 781357 or 782106 and serial numbers listed in the recall (many starting with 46000 through 46289).
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-1570-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1570-2024 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.
