Philips recalls Intera 1.0T Omni/Stellar 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 1.0T 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.
An incorrectly installed patient support table floor plate could cause the table to become unstable during MRI scans. This might lead to patient injury if the table shifts or falls during use.
Healthcare facilities using Philips Intera 1.0T Omni/Stellar 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 include specific serial numbers listed in the recall notice: 7069, 7213, 7238, 10045, 7248, 10341, 10073, 7020, 7247, 7081, 7141, 7120, 7116, 10334, 10047, 7226, 7111, 7203, 7117, 7022, 7031, 7085, 7051, 7156, 7215, 10001, 10328, 7018.
Look for the serial number on the device label to determine if your unit is affected.
Reach out to Philips directly for instructions on repair or replacement of the affected table floor plate.
The patient support table floor plate may be incorrectly installed, which could cause instability during MRI scans and lead to patient injury.
Check the serial number on the device label. Affected units have specific serial numbers listed in the recall notice.
Contact Philips directly for instructions on repair or replacement of the affected 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-1573-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1573-2024 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.
