Philips recalls SmartPath to Ingenia Elition X MRI systems due to potential fire risk from loose g-MDU connections. Affected units may require repair to prevent smoke/fire alarms in hospital technical rooms.
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 SmartPath to Ingenia Elition X MRI systems because loose connections in the power unit could cause smoke or fire alarms in hospital technical rooms. This poses a fire risk in medical facilities where these systems are used.
Loose connections in the g-MDU (global Mains Distribution Unit) L3 terminal can create electrical hotspots. These hotspots may trigger smoke or fire alarms in hospital technical rooms, potentially causing disruptions or safety issues.
Hospital facilities using Philips SmartPath to Ingenia Elition X MRI systems are most at risk. The recall affects specific model units with the serial number 42194.
Check for the model number 782118 and serial number 42194 on the system. This recall applies to specific MRI systems sold by Philips North America.
Inspect the g-MDU L3 terminal connection for looseness. If loose, contact Philips for repair instructions.
Loose connections in the g-MDU L3 terminal may create electrical hotspots that trigger smoke or fire alarms in hospital technical rooms.
Check if your system has the model number 782118 and serial number 42194. Contact Philips for repair instructions if the connection appears loose.
The recall describes potential smoke or fire alarms but does not mention direct injury risks. The hazard is limited to technical room alarms.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1863-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1863-2024 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.
