Philips recalls Ingenia Ambition S MRI model 781359 due to potential mechanical failure in hoisting blocks during decommissioning. Affected units have specific serial numbers listed in the recall notice.
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 its Ingenia Ambition S MRI system model 781359 because hoisting blocks that move the magnet during decommissioning have a mechanical issue. This could lead to safety risks if the magnet isn't handled properly during moving activities.
The MRI magnet has 4 lifting blocks designed to be moved by cranes during decommissioning or relocation. A mechanical issue detected in these blocks could cause failure during handling, potentially leading to safety hazards if not addressed.
Medical facilities using the Ingenia Ambition S MRI system model 781359 are affected. Staff handling the magnet during decommissioning or moving activities are at higher risk due to the mechanical issue.
Check for the model number 781359 on the MRI system. Affected units have specific serial numbers listed in the recall notice, including numbers starting with 48000 through 48198.
Review the serial numbers listed in the recall notice to confirm if your unit is affected.
The recall indicates a mechanical issue with hoisting blocks during decommissioning, but the system is safe for regular medical use. Affected units require specific handling procedures.
The recall does not specify a remedy, so contact Philips directly for guidance on next steps.
Check the serial numbers listed in the recall notice, which include numbers starting with 48000 through 48198 for model 781359.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1796-2021 — Philips Philips Hello, I own a Philips that is covered by recall Z-1796-2021 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.
