Philips recalls Ingenia Ambition S MRI systems with potentially incorrectly installed patient support table floor plates. Affected units have specific model and serial numbers; users should contact Philips for details.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Ingenia Ambition 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 MRI procedures. This instability might lead to the table shifting or moving unexpectedly, potentially causing injury to the patient or staff.
Healthcare facilities using the Ingenia Ambition S MRI systems with the listed model and serial numbers are most at risk. Patients undergoing MRI scans on these systems may face safety concerns if the table isn't correctly installed.
Check if your MRI system model is 782133, 782139, 781359, or 782108. Look for the specific serial numbers listed in the recall notice. The UDI-DI numbers also match the provided list.
Reach out to Philips directly using the contact information provided in the recall notice to confirm if your unit is affected and to get instructions for correction.
Check if your model number is 782133, 782139, 781359, or 782108, and if your serial number is in the list provided in the recall notice.
Contact Philips directly to determine if your unit is affected and to receive instructions for correction.
The recall notice does not specify how to verify the installation; contact Philips for details.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1568-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1568-2024 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.
