Philips recalls Intera CV MRI systems with potentially incorrectly installed patient support table floor plates. Affected units include specific serial numbers. Correct installation is critical for safety during procedures.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera CV MRI systems due to a risk that 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 procedures. This instability might lead to patient injury if the table shifts unexpectedly.
Healthcare facilities using Philips Intera CV 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 device label. Affected units have serial numbers 8528, 8653, 8907, 8869, 8703, 9017, 8756, or 8014.
Verify that the patient support table floor plate is installed correctly according to Philips guidelines.
Philips recalls Intera CV MRI systems with potentially incorrectly installed patient support table floor plates.
Serial numbers 8528, 8653, 8907, 8869, 8703, 9017, 8756, and 8014.
Check the serial number on the device label. Affected units have the specific serial numbers listed above.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1586-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1586-2024 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.
