Philips recalls Achieva 1.5T MRI systems with potentially incorrectly installed patient support table floor plates. This could cause safety issues during medical procedures. Affected units have specific model and serial numbers.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Achieva 1.5T MRI systems because the patient support table floor plate might be installed incorrectly. This could lead to safety risks 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 patient injury if the table moves unexpectedly while the patient is being scanned.
Healthcare facilities using Philips Achieva 1.5T MRI systems with model numbers 781283 or 781346 are most at risk. Patients undergoing MRI scans with these systems may face safety issues if the table isn't properly installed.
Check for model numbers 781283 or 781346 on the Achieva 1.5T MRI system. The affected units also have specific serial numbers listed in the recall notice.
Verify that the patient support table floor plate is installed correctly according to Philips' instructions.
Reach out to Philips customer support for guidance on verifying the table installation and potential remedies.
Model numbers 781283 and 781346 are affected.
Check the model number on your Achieva 1.5T MRI system. Affected units also have specific serial numbers listed in the recall notice.
No, but you should verify the table installation is correct before continuing use.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1551-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1551-2024 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.
