Philips recalls Intera 1.5T MRI systems with potentially incorrectly installed patient support table floor plates. Affected models include specific serial numbers. Users should contact Philips for details.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera 1.5T MRI systems because the patient support table floor plate may be incorrectly installed. 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 MRI scans. This instability might lead to patient injury if the table shifts or moves unexpectedly during procedures.
Healthcare facilities using Philips Intera 1.5T MRI systems with the affected serial numbers are most at risk. Patients undergoing scans with these systems may face safety concerns if the table isn't correctly installed.
Check if your Intera 1.5T MRI system has model numbers 781195 or 781295. Look for specific serial numbers listed in the recall notice, which include a long list of numbers starting with 18501 and ending with 30315.
Reach out to Philips directly to confirm if your specific model and serial number are affected by this recall.
The affected models are Philips Intera 1.5T MRI systems with model numbers 781195 or 781295 and specific serial numbers listed in the recall notice.
Check your system's model number (781195 or 781295) and serial number against the list of affected serial numbers provided in the recall notice.
Contact Philips directly to confirm if your system is affected and follow their instructions for 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-1575-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1575-2024 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.
