Philips recalls MR 5300 MRI systems with potentially incorrectly installed patient support table floor plates. This could lead to 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 MR 5300 MRI systems because the patient support table floor plate might be installed incorrectly. This could cause safety problems 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 procedures. This instability might lead to the table moving unexpectedly, potentially causing injury to patients or staff.
Medical facilities that own or use Philips MR 5300 MRI systems with the listed serial numbers are most at risk. Patients undergoing MRI scans could face safety issues if the table isn't properly installed.
Check if your Philips MR 5300 MRI system has a serial number listed in the provided list of numbers (e.g., 63029, 63087, 63014, etc.). The system model is MR 5300 with specific serial numbers.
Verify if your MRI system has a serial number listed in the provided list of numbers (e.g., 63029, 63087, 63014, etc.).
The patient support table floor plate may be incorrectly installed, which could cause the table to become unstable during MRI procedures.
Check if your system has a serial number listed in the provided list of numbers (e.g., 63029, 63087, 63014, etc.).
The recall requires checking if your system has a serial number in the list. If it does, contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1587-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1587-2024 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.
