Philips recalls Ingenia 1.5T S MRI scanners with specific serial numbers due to a loose connection that could cause smoke or fire in hospital technical rooms. Affected units must be checked by authorized personnel.
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 1.5T S MRI scanners because a loose electrical connection might create a fire hazard in hospital technical rooms. This could lead to smoke or fire alarms, potentially disrupting critical medical operations.
The g-MDU terminal connection may become loose, creating a hotspot that can trigger smoke or fire alarms in hospital technical rooms. This could lead to unintended shutdowns or safety alerts during critical medical procedures.
Hospital facilities using the recalled Ingenia 1.5T S MRI scanners with specific serial numbers are most at risk. Patients and staff could face disruptions if the scanner malfunctions.
Check if your scanner has the model number 781347 and serial numbers listed in the recall notice. The serial numbers include specific combinations like 81003, 81050, 81051, and others.
Reach out to Philips customer support to verify if your scanner is affected by the recall.
The recall addresses a potential fire hazard in hospital technical rooms, but the risk is not immediate. Affected units require professional evaluation.
Check the serial numbers listed in the recall notice, which include specific combinations like 81003, 81050, 81051, and others.
No, but affected units should be checked by authorized personnel to ensure safety.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1847-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1847-2024 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.
