Philips recalls Ingenia Ambition X MRI systems with model numbers 781356 and 782109 due to potential mechanical issues in hoisting blocks that could affect safe decommissioning or moving.
The MR magnet is equipped with 4 lifting blocks, which are positioned on top of the magnet. These blocks are used to allow the magnets to be moved in or out by a lifting crane, e.g. during decommissioning or moving activities. A mechanical issue was detected on these hoisting interface blocks on top of the magnet.
Philips is recalling specific models of their Ingenia Ambition X MRI systems because hoisting blocks used for moving the magnets have a mechanical issue. This could lead to problems during decommissioning or moving activities, though the recall does not specify immediate safety risks to users.
The MRI system's magnet has 4 lifting blocks designed for moving during decommissioning or relocation. A mechanical issue detected in these blocks could cause problems during handling activities, but the recall does not specify how this might impact safety during normal operation.
Healthcare facilities that own or use the recalled Ingenia Ambition X MRI systems with model numbers 781356 or 782109 are most at risk. The recall affects specific serial numbers listed in the notice.
Check for model numbers 781356 or 782109 on the MRI system. The specific serial numbers listed in the recall notice (e.g., 47001, 47002, etc.) indicate affected units. Note that some serial numbers were removed from scope as of November 2023.
Identify if your MRI system has model numbers 781356 or 782109.
Philips detected a mechanical issue in the hoisting blocks used for moving the magnet during decommissioning or relocation activities.
The recall includes specific serial numbers listed in the notice, such as 47001, 47002, 47003, and others. Some serial numbers were removed from scope as of November 2023.
The recall does not specify immediate safety risks during normal operation, so there is no need to stop using it now. However, affected units should be checked for the model and serial numbers.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1795-2021 — Philips Philips Hello, I own a Philips that is covered by recall Z-1795-2021 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.
