Philips recalls Intera 0.5T MRI systems with potentially incorrectly installed patient support table floor plates. Affected units have specific serial numbers; contact Philips for repair or replacement.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera 0.5T 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 is not 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 moves unexpectedly.
Healthcare facilities using the recalled Intera 0.5T MRI systems are most at risk. Patients undergoing MRI scans with these systems could face safety issues if the table is not correctly installed.
Check the serial numbers on the system: 6047, 6018, 6023, 6027, 6031, 6044, 6060, 10306, 6015, 6061, 6025, 6054, 6001, 6066. The product is a Philips Intera 0.5T Standard MRI system.
Verify the serial number on your system to confirm if it is listed among the affected numbers: 6047, 6018, 6023, 6027, 6031, 6044, 6060, 10306, 6015, 6061, 6025, 6054, 6001, 6066.
Reach out to Philips North America for guidance on the repair or replacement of the patient support table floor plate.
The patient support table floor plate may be incorrectly installed, which could cause instability during MRI scans and potentially lead to patient injury.
Check the serial number on your system; affected units have specific serial numbers: 6047, 6018, 6023, 6027, 6031, 6044, 6060, 10306, 6015, 6061, 6025, 6054, 6001, 6066.
Contact Philips North America for instructions on repairing or replacing the patient support table floor plate.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1572-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1572-2024 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.
