Philips recalls Ingenia Ambition S MRI machines with specific model numbers due to potential loose connections that could cause smoke or 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 certain Ingenia Ambition S MRI machines because a loose connection in the power unit might cause smoke or fire alarms in hospital technical rooms. This could lead to false alarms or actual fire hazards in critical hospital environments.
The g-MDU (global Mains Distribution Unit) L3 terminal connection can become loose, creating a hotspot. This hotspot may trigger smoke or fire alarms in the hospital's technical room, potentially causing false alarms or actual fire hazards.
Hospital facilities using the recalled Ingenia Ambition S MRI models are most at risk. Patients and staff in hospitals with these machines may experience false fire alarms or potential fire hazards.
Check the model numbers: 782139, 782133, 782108, or 781359. The serial numbers listed in the recall include a range of numbers starting with 48000 through 48893.
Identify if your machine has model numbers 782139, 782133, 782108, or 781359.
Reach out to Philips customer support for further assistance with the recall.
The g-MDU L3 terminal connection may become loose, creating a hotspot that could trigger smoke or fire alarms in hospital technical rooms.
Check if your machine has model numbers 782139, 782133, 782108, or 781359. Contact Philips for further instructions.
The recall states the hazard could cause smoke or fire alarms, but does not specify a risk of serious injury to people.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1850-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1850-2024 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.
