Philips recalls Enterprise 1.5T MRI systems with potentially incorrectly installed patient support table floor plates. This could cause safety issues during medical procedures. Affected units have specific serial numbers listed in the recall notice.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Enterprise 1.5T MRI systems because the patient support table floor plate might be installed incorrectly. This could lead to safety risks 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 instability might lead to injuries or safety hazards for patients and staff.
Healthcare facilities using the affected Philips Enterprise 1.5T MRI systems are likely impacted. Medical staff and patients using these systems could be at risk if the floor plate is not correctly installed.
Check the serial numbers listed in the recall notice: 10709, 10682, 10678, 10729, 10217, 10031, 10092, 10111, 10715, 10074, 10121, 10122, 10119, 10732, 10775, 10795, 10041, 10711, 10144, 10792, 10787, 10689, 10218, 10704, 10693, 10685, 10696, 10687, 10726, 10797, 10799, 10789, 10790. The affected units are part of the Enterprise 1.5T MRI system with model number 781145.
Verify that the patient support table floor plate is installed correctly according to the manufacturer's guidelines.
The affected model number is 781145.
The affected serial numbers are 10709, 10682, 10678, 10729, 10217, 10031, 10092, 10111, 10715, 10074, 10121, 10122, 10119, 10732, 10775, 10795, 10041, 10711, 10144, 10792, 10787, 10689, 10218, 10704, 10693, 10685, 10696, 10687, 10726, 10797, 10799, 10789, 10790.
No, but you should check the floor plate installation to ensure it is correct. The recall does not require immediate discontinuation of use.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1557-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1557-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
