Philips recalls Intera 1.5T Achieva Nova MRI systems with potentially incorrectly installed patient support table floor plates. Affected units have specific serial numbers; contact Philips for details.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera 1.5T Achieva Nova 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 MRI scans. This instability might lead to injuries if the table shifts or falls during patient positioning.
Healthcare facilities using Philips Intera 1.5T Achieva Nova MRI systems with specific serial numbers are affected. Medical staff and patients using these systems are at risk if the table floor plate is not correctly installed.
Check the serial number on the patient support table floor plate for the listed numbers: 12144, 12075, 12031, 12015, 12056, 12051, 12107, 12078, 12065, 12045, 12046, 12026, 12105, 12062, 12111, 12077, 12044, 12049, 12119, 12081, 12161, 12099, 12138, 12020, 12139, 12102, 12069, 12152, 12004, 12086, 12122, 12128, 12052, 12063, 12005, 12050, 12141, 12025, 12106, 12146, 12001, 11010, 12074, 12073, 12079, 12057.
Verify the serial number on the patient support table floor plate against the list of affected serial numbers provided in the recall notice.
The patient support table floor plate may be incorrectly installed, which could cause instability during MRI scans and potentially lead to injuries.
Check the serial number on the patient support table floor plate for the listed numbers: 12144, 12075, 12031, 12015, 12056, 12051, 12107, 12078, 12065, 12045, 12046, 12026, 12105, 12062, 12111, 12077, 12044, 12049, 12119, 12081, 12161, 12099, 12138, 12020, 12139, 12102, 12069, 12152, 12004, 12086, 12122, 12128, 12052, 12063, 12005, 12050, 12141, 12025, 12106, 12146, 12001, 11010, 12074, 12073, 12079, 12057.
Contact Philips directly for instructions on how to verify the installation and any necessary corrective actions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1577-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1577-2024 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.
