Philips recalls Intera 1.5T Explorer/Nova Dual MRI systems with potentially incorrectly installed patient support table floor plates. Affected units have specific serial numbers; contact Philips for details.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera 1.5T 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 isn't properly secured.
The patient support table floor plate may be incorrectly installed, which could cause the table to shift or become unstable during MRI scans. This instability might lead to patient injury if the table moves unexpectedly during the procedure.
Medical facilities using the recalled Intera 1.5T Explorer/Nova Dual MRI systems are most at risk. Patients undergoing scans with these systems could face safety issues if the table floor plate is not correctly installed.
Check the serial numbers listed: 8918, 10035, 8803, 10037, 9025, 10022, 10638, 10640, 8743, 8651, 10091, 8690. The affected models are Philips Intera 1.5T Explorer/Nova Dual MRI systems.
Verify your system's serial number against the list: 8918, 10035, 8803, 10037, 9025, 10022, 10638, 10640, 8743, 8651, 10091, 8690.
The patient support table floor plate may be incorrectly installed, which could cause the table to shift or become unstable during MRI scans.
Check the serial number against the list: 8918, 10035, 8803, 10037, 9025, 10022, 10638, 10640, 8743, 8651, 10091, 8690.
The recall record does not specify a remedy, so contact Philips directly for instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1579-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1579-2024 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.
