Philips recalls Ingenia Ambition X MRI systems with incorrectly installed patient support table floor plates. Affected units have specific model and serial numbers. Correct installation is critical for safety during medical procedures.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Ingenia Ambition X MRI machines because the patient support table floor plate may be incorrectly installed. 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 MRI procedures. This instability might lead to patient injury if the table shifts or moves unexpectedly while the patient is being scanned.
Healthcare facilities using Philips Ingenia Ambition X MRI systems with the affected model or serial numbers are most at risk. Patients undergoing MRI scans with these systems could face safety issues if the table is not correctly installed.
Check the model numbers: 781359, 782109, or 782138. Look for the UDI-DI numbers: 884838090040, 884838098350, or 884838108622. The serial numbers listed in the recall are specific numbers starting with 47000 and ending with 47798.
Verify that the patient support table floor plate is installed correctly according to Philips' instructions.
No, but you should check if your machine has the affected model or serial numbers listed in the recall. If it does, ensure the patient support table floor plate is installed correctly.
Contact Philips directly to confirm if your machine is affected and follow their instructions for proper installation of the patient support table floor plate.
Check the model numbers (781359, 782109, 782138) or UDI-DI numbers (884838090040, 884838098350, 884838108622) on your machine. If your serial number matches the list provided in the recall, it is affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1569-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1569-2024 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.
