Philips recalls specific Intera 1.5T MRI systems due to potential incorrect installation of patient support table floor plates, which could lead to safety issues during medical procedures.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera 1.5T MRI systems because the patient support table floor plate might be installed incorrectly. This could cause safety risks during medical procedures if the table is not properly secured.
The patient support table floor plate may be incorrectly installed, which could lead to the table becoming unstable during medical procedures. This instability might cause the table to shift or move unexpectedly, potentially causing injury to the patient.
Medical facilities that own or use the recalled Intera 1.5T MRI systems are most at risk. Patients undergoing scans with these systems may face safety issues if the table is not correctly installed.
Check for the model number 781104 on the Intera 1.5T Omni/Stellar MRI systems. The serial numbers listed in the recall include 8483, 8526, 8257, 8171, 8731, and others.
Verify that the patient support table floor plate is installed correctly according to the manufacturer's instructions.
The patient support table floor plate may be incorrectly installed, which could lead to instability during medical procedures and potential injury.
The affected model number is 781104 for the Intera 1.5T Omni/Stellar MRI systems.
Check the serial numbers listed in the recall: 8483, 8526, 8257, 8171, 8731, 8126, 10403, 10401, 10410, 10407, 8266, 8286, 8246, 8725, 8556, 8338, 8625, 8516, 8332, 8138, 8921, 8359.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1581-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1581-2024 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.
