Philips recalls Ingenia Ambition X MRI systems with model numbers 782138, 782109, and 781356 due to a loose g-MDU terminal that could cause 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 Ingenia Ambition X MRI systems that may have a loose electrical connection causing smoke or fire alarms in hospital technical rooms. This could lead to fire hazards if the connection becomes loose.
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose, creating a hotspot that can cause smoke or fire alarms in the hospital's technical room. This could lead to fire hazards if the connection is not secure.
Hospital facilities using Philips Ingenia Ambition X MRI systems with model numbers 782138, 782109, or 781356 are most at risk. The recall affects medical equipment installed in hospitals.
Check for model numbers 782138, 782109, or 781356 on the system. The recall applies to MRI systems sold in the U.S. by Philips North America.
Inspect the g-MDU L3 terminal connection for looseness; if loose, contact Philips for assistance.
The recall states that a loose connection may cause smoke or fire alarms in hospital technical rooms, but it does not specify that fire will occur. The hazard is potential for alarms, not immediate fire.
Check for model numbers 782138, 782109, or 781356 on the system. The recall applies to MRI systems sold in the U.S. by Philips North America.
The recall does not specify a remedy; Philips has not provided instructions for fixing the issue. Contact Philips directly for assistance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1851-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1851-2024 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.
