Philips recalls Intera 1.0T Power/Pulsar MRI systems with potentially incorrectly installed patient support table floor plates. Affected models include specific serial numbers; users should contact Philips for details.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera 1.0T Power/Pulsar MRI systems due to a risk that 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 medical procedures. This instability might lead to patient injury if the table shifts unexpectedly.
Healthcare facilities using the recalled Intera 1.0T Power/Pulsar MRI systems are most at risk. Patients undergoing scans with these systems may be affected if the table is not correctly installed.
Check the serial numbers listed: 7062, 7164, 7102, 7113, 7084, 10381, 7097, 10383, 10391, 7150, 7074, 7237, 7190, 7198, 10413, 10382, 7103, 10071. The product is sold under Philips North America LLC.
Verify if your MRI system has one of the listed serial numbers: 7062, 7164, 7102, 7113, 7084, 10381, 7097, 10383, 10391, 7150, 7074, 7237, 7190, 7198, 10413, 10382, 7103, 10071.
The patient support table floor plate may be incorrectly installed, which could cause instability during medical procedures.
Check the serial numbers listed: 7062, 7164, 7102, 7113, 7084, 10381, 7097, 10383, 10391, 7150, 7074, 7237, 7190, 7198, 10413, 10382, 7103, 10071.
Contact Philips directly for instructions on verifying and addressing the issue with the patient support table floor plate.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1574-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1574-2024 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.
