Philips recalls Ingenia 1.5T S 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 Ingenia 1.5T S 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 shifts unexpectedly while a patient is being scanned.
Healthcare facilities using the recalled MRI systems are most at risk. Patients undergoing scans with these systems may face safety concerns if the table isn't correctly installed.
Check the serial number on the device. Affected units have specific serial numbers listed in the recall notice, including 81034, 81033, 81015, and many others.
Verify the serial number against the list provided in the recall notice to determine if your device is affected.
Reach out to Philips directly for guidance on whether your device needs correction or repair.
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 against the list of affected numbers provided in the recall notice, which includes specific serial numbers like 81034, 81033, and 81015.
No, but you should check the serial number and contact Philips to determine if your device needs correction or repair.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1565-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1565-2024 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.
