Philips recalls Intera Achieva 1.5T Pulsar MRI systems with potentially incorrectly installed patient support table floor plates. This could lead to safety issues during medical procedures. Affected units have specific serial numbers listed in the recall notice.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Intera Achieva 1.5T Pulsar MRI systems because the patient support table floor plate might be installed incorrectly. This could cause safety problems 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 move or shift, potentially affecting patient safety.
Healthcare facilities that own or use the recalled MRI systems are most at risk. Patients undergoing scans with these systems may face safety issues if the table is not correctly installed.
Check the serial numbers on the system: 11069, 11024, 11048, 11090, 11049, 11058, 11013, 11036, 11045, 11087, 11061, 11009, 11060, 11044, 11039, 11043, 11020, 11007, 11025, 11094, 11033, 11059, 11019, 11068.
Verify that the patient support table floor plate is installed correctly according to the manufacturer's guidelines.
The recalled model is Philips Intera Achieva 1.5T Pulsar MRI system with specific serial numbers listed in the recall notice.
Check the serial numbers on your system: 11069, 11024, 11048, 11090, 11049, 11058, 11013, 11036, 11045, 11087, 11061, 11009, 11060, 11044, 11039, 11043, 11020, 11007, 11025, 11094, 11033, 11059, 11019, 11068.
The recall does not specify a remedy, so you should check with Philips North America LLC for guidance on verifying and correcting the installation.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1585-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1585-2024 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.
