Philips recalls Evolution 3.0T MRI machines with potential loose RF carrier screws that could block tabletop movement, causing delays in diagnosis and patient anxiety.
Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May lead to delay in diagnosis and/or may include anxiety of a patient is left on the tabletop inside the bore for a longer duration than anticipated. movement.
Philips is recalling certain Evolution 3.0T MRI machines because screws in the RF carrier assembly might become loose and block the tabletop movement. This could delay diagnoses and cause patient anxiety if the patient remains on the table longer than expected.
Screws in the RF carrier assembly can become loose and protrude beyond the surface, potentially blocking the horizontal tabletop movement. This may cause delays in diagnosis and leave patients on the table longer than anticipated, causing anxiety.
MRI machine users and healthcare facilities that own or operate the recalled Evolution 3.0T MRI systems. Patients undergoing scans may experience longer wait times or anxiety if the machine malfunctions.
Check for serial numbers 85675, 85687, or 85695 on the machine's label. The product was sold with model numbers 782117 or 782143.
Inspect the RF carrier assembly for screws that protrude beyond the surface.
Reach out to Philips customer support for specific model information and next steps.
Screws in the RF carrier assembly may become loose and protrude, potentially blocking tabletop movement which could delay diagnoses and cause patient anxiety.
Model numbers 782117 and 782143 with serial numbers 85675, 85687, or 85695.
No, but you should check for loose screws and contact Philips for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3193-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-3193-2024 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.
