Philips recalls Intera 1.5T Power/Pulsar MRI systems with potentially incorrectly installed patient support table floor plates. This could cause safety issues during medical procedures. Affected units have specific serial numbers.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera 1.5T Power/Pulsar 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 medical procedures. This instability might lead to injuries if the table moves unexpectedly while a patient is being scanned.
Medical facilities that own or use the recalled Intera 1.5T Power/Pulsar MRI systems are most at risk. Patients undergoing scans with these systems could face safety issues if the table isn't properly installed.
Check the serial number on the system's label. Affected units have specific serial numbers listed in the recall notice, including 8342, 8104, 8899, and other numbers.
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 cause the table to become unstable during medical procedures.
Check the serial number on the system's label. Affected units have specific serial numbers listed in the recall notice, including 8342, 8104, 8899, and other numbers.
No. The recall requires checking the installation of the patient support table floor plate. There is no immediate need to stop using the system.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1582-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1582-2024 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.
