Philips recalls Ingenia Elition X MRI machines with loose RF carrier screws that could block tabletop movement, causing delays in diagnosis and patient anxiety. Affected units have specific serial numbers and model codes.
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 Ingenia Elition X MRI machines because screws in the radio frequency carrier assembly might become loose and protrude, potentially blocking the tabletop movement. This could delay diagnosis and cause patient anxiety if the machine is left running longer than expected.
The screws in the radio frequency carrier assembly can become loose and protrude beyond the surface, which might block the horizontal tabletop movement. This could lead to delays in diagnosis and cause patients to remain on the table longer than intended, increasing anxiety.
Medical facilities using Philips Ingenia Elition X MRI machines with serial numbers listed in the recall notice are affected. Patients undergoing scans may experience delays or anxiety if the machine malfunctions.
Check if your machine has serial numbers 26500-62188 or 66001-66002. Model numbers 782151, 782119, 781358, 782107, or 782136 are also affected.
Verify your machine's serial number against the list provided in the recall notice: 26500, 26505, 28502, 28509, 45393, 45467, 45599, 62029, 62041, 62051, 62052, 62061, 62066, 62070, 62071, 62081, 62082, 62083, 62091, 62103, 62111, 62113, 62114, 62120, 62126, 62129, 62147, 62148, 62186, 62187, 62188, 66001, 66002.
The screws in the radio frequency carrier assembly may become loose and protrude, potentially blocking the tabletop movement and causing delays in diagnosis or patient anxiety.
Model numbers 782151, 782119, 781358, 782107, and 782136 are affected.
Check your machine's serial number against the list: 26500, 26505, 28502, 28509, 45393, 45467, 45599, 62029, 62041, 62051, 62052, 62061, 62066, 62070, 62071, 62081, 62082, 62083, 62091, 62103, 62111, 62113, 62114, 62120, 62126, 62129, 62147, 62148, 62186, 62187, 62188, 66001, 66002.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3200-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-3200-2024 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.
