Philips recalls Ingenia Ambition X MRI systems with Model No. 782109 due to a potentially dangerous incorrect electrical shock warning label that could risk electrical shock for service personnel.
An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.
Philips is recalling Ingenia Ambition X MRI systems with Model No. 782109 because an incorrect electrical shock warning label may be present on the Liquid Cooling Cabinet. This could pose a risk of electrical shock for service personnel who work on the system.
The incorrect label has a white background instead of yellow and is missing the high voltage warning symbol. This could lead to service personnel receiving an electrical shock during maintenance work on the MRI system.
Service personnel who work on the Ingenia Ambition X MRI systems with Model No. 782109 are most at risk. The recall affects specific units sold in the U.S. market.
Check for the model number 782109 on the MRI system. The recall includes units with Serial Number 47785 and UDI-DI 00884838098350.
Inspect the Liquid Cooling Cabinet for the incorrect electrical shock warning label with a white background instead of yellow.
Philips recalls Ingenia Ambition X MRI systems with Model No. 782109 because an incorrect electrical shock warning label may be present on the Liquid Cooling Cabinet, which could risk electrical shock for service personnel.
If you own an Ingenia Ambition X MRI system with Model No. 782109, check the Liquid Cooling Cabinet for the incorrect label. Contact Philips for further instructions.
The recall record does not specify a fix or remedy for the label issue.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0810-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0810-2024 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.
