Philips recalls specific MR systems due to a loose connection risk in hospital technical rooms that could cause smoke or fire alarms. Affected models include 781440 with serial numbers 70980 and 71569.
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 MRI systems because a loose electrical connection could cause smoke or fire alarms in hospital technical rooms. This hazard affects specific models with serial numbers 70980 and 71569.
A loose connection in the global Mains Distribution Unit (L3 terminal) can create a hotspot. This may trigger smoke or fire alarms in hospital technical rooms, but does not indicate an immediate fire risk.
Hospital staff and technicians who use these MRI systems are most at risk. The recall applies to specific models sold in the U.S. with serial numbers 70980 and 71569.
Check for model number 781440 with serial numbers 70980 or 71569. These MRI systems were sold in the U.S. by Philips North America.
Inspect the global Mains Distribution Unit (L3 terminal) for loose connections. If loose, contact Philips for a fix.
The recall indicates a potential for smoke or fire alarms in hospital technical rooms, but does not confirm an immediate fire risk.
Check for model number 781440 with serial numbers 70980 or 71569. These specific units were sold in the U.S. by Philips.
Inspect the L3 terminal connection. If loose, contact Philips for a fix. There is no immediate need to stop using the system.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1859-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1859-2024 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.
