Philips recalls Achieva 1.5T MRI machines with specific serial numbers due to potential smoke and fire from Gradient Coil component failure. Affected units include models with Product Numbers 781178, 781196, 781296, 781343 and serial numbers listed in the recall notice.
Potential component failure in the Gradient Coil could product smoke and/or fire.
Philips is recalling certain Achieva 1.5T MRI machines because a component called the Gradient Coil could fail and produce smoke or fire. This recall affects specific product numbers and serial numbers listed in the notice. If you own one of these models, you should stop using it immediately.
The Gradient Coil component in the MRI machine has a potential failure that could cause it to produce smoke or fire. This hazard occurs during normal operation and could lead to serious injury or property damage if the component fails.
MRI machine owners who purchased the affected Achieva 1.5T models between 2021 and 2023. Patients and staff using these machines are at risk of smoke or fire if the component fails.
Check if your Achieva 1.5T MRI has Product Numbers 781178, 781196, 781296, or 781343. Also, verify your serial number is listed in the detailed list provided in the recall notice.
Immediately stop using the affected Achieva 1.5T MRI machine if you own one of the recalled models.
The affected models include Achieva 1.5T MRI machines with Product Numbers 781178, 781196, 781296, 781343 and specific serial numbers listed in the recall notice.
Check your machine's Product Number and serial number against the list provided in the recall notice. Affected units have Product Numbers 781178, 781196, 781296, 781343 and specific serial numbers listed in the notice.
Immediately stop using the affected Achieva 1.5T MRI machine and contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0389-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0389-2024 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.
