Philips recalls Intera 1.5T Master/Nova MRI systems with potentially incorrectly installed patient support table floor plates. This could affect safety 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 Master/Nova 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 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 patient injury if the table moves unexpectedly while a patient is being scanned.
Medical facilities using Philips Intera 1.5T Master/Nova MRI systems with the listed serial numbers are most at risk. Patients undergoing scans with these systems could be affected if the table isn't properly installed.
Check the serial number on the patient support table of your Intera 1.5T Master/Nova MRI system. Affected units have specific serial numbers listed in the recall notice, including 8648, 8650, and many others.
Verify the serial number on the patient support table to see if it matches the list of affected serial numbers provided in the recall.
The patient support table floor plate may be incorrectly installed, which could cause instability during medical procedures and potentially lead to patient injury.
Check the serial number on the patient support table to see if it matches the list of affected serial numbers provided in the recall notice. If it does, contact Philips for further instructions.
Affected units have specific serial numbers listed in the recall notice, including 8648, 8650, and many others. Check the serial number on your patient support table.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1580-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1580-2024 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.
