Philips recalls Intera 1.5T R11 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 Intera 1.5T R11 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 if the table moves unexpectedly.
Healthcare facilities using the recalled Intera 1.5T R11 MRI systems are most at risk. Patients undergoing scans with these systems could face safety issues if the table isn't correctly installed.
Check the serial numbers listed in the recall notice: 18070, 18021, 18025, 18110, 18019, 18009, 18055, 18064, 18095, 18105, 18002, 18082, 18083, 18039, 18108, 18032, 18071, 18092, 18074, 18030, 18011, 18049, 18066, 18097, 18031. The product is a 1.5T Magnetic Resonance System from Philips.
Verify if your Intera 1.5T R11 MRI system has a serial number from the list provided in the recall notice.
The patient support table floor plate may be incorrectly installed, which could cause instability during medical procedures.
Check if your system has a serial number from the list provided in the recall notice. If it does, contact Philips for further instructions.
The recall indicates a potential safety risk if the table is not properly installed, but the exact risk level isn't specified in the notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1583-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1583-2024 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.
