Philips recalls Achieva 3.0T PET-MR systems due to potential fire risk from loose electrical connections in hospital technical rooms. Affected units have specific serial numbers and model numbers.
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
Philips is recalling certain Achieva 3.0T PET-MR systems because loose electrical connections could cause smoke or fire in hospital technical rooms. This is a serious hazard that requires immediate attention to prevent fire risks.
The g-MDU (global Mains Distribution Unit) L3 terminal connection can become loose, creating a hotspot that may lead to smoke or fire alarms in the hospital's technical room. This hazard occurs during normal operation and could cause significant fire risks in medical facilities.
Hospitals and medical facilities that own the recalled Achieva 3.0T PET-MR systems with serial numbers starting with 43006 are most at risk. These systems are used for diagnostic imaging in medical settings.
Check for the model number 781477 and serial numbers starting with 43006 on the Achieva 3.0T PET-MR systems. These units were sold by Philips North America.
Immediately disconnect the system from power and do not use the affected Achieva 3.0T PET-MR systems until further instructions are received.
The model number is 781477.
Serial numbers starting with 43006.
Check for the model number 781477 and serial numbers starting with 43006 on the Achieva 3.0T PET-MR systems.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1840-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1840-2024 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.
