Philips recalls SmartPath to dStream 1.5T MRI machines with loose RF carrier screws that could block the horizontal tabletop, 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 SmartPath to dStream 1.5T MRI machines because screws in the RF carrier assembly might become loose and protrude, potentially blocking the tabletop. This could delay diagnoses and cause patient anxiety by leaving them on the table longer than expected.
The RF carrier assembly screws may loosen and stick out, which could block the horizontal tabletop. This might delay diagnosis and cause patients to stay on the table longer than intended, leading to anxiety.
Patients and medical staff using Philips SmartPath to dStream 1.5T MRI machines with specific serial numbers are affected. Those who use the machines for diagnostic imaging are most at risk.
Check for the serial numbers listed: 8876 10190 10521 13021 13023 18520 18892 18942 20159 21127 21158 21513 21726 21803 22027 22048 22093 22247 30054 32250 32355 32412 32419 32469 32539 32724 32827 33371 33639 39070 75067. The product is a 1.5T MRI diagnostic device for cross-sectional and spectroscopic imaging.
Look for the listed serial numbers on the device to confirm if it is affected.
The RF carrier assembly screws may become loose and protrude, potentially blocking the horizontal tabletop, which could delay diagnosis and cause patient anxiety.
Check the serial numbers listed in the recall notice to see if your device is affected. If it is, contact Philips for further instructions.
The recall states the screws could block the tabletop, leading to delays and patient anxiety, but does not mention serious injury risks.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3203-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-3203-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
