Philips recalls Ingenia 1.5T MRI systems with specific model numbers due to potential delay in patient evacuation during manual mode use, which could affect treatment timing. Affected units have model numbers listed in the recall.
When using manual mode, the tabletop may not completely move in or out and result in potential delay in patient evacuation from the bore, which could result in a delay of treatment
Philips is recalling certain Ingenia 1.5T MRI systems that may not move the tabletop completely in or out during manual mode use. This could delay patient evacuation from the MRI bore, potentially causing treatment delays. The recall does not require immediate stop use but requires checking model numbers.
When the MRI system is in manual mode, the tabletop may not move fully in or out of the MRI bore. This can delay patient evacuation, which might cause treatment delays if the patient needs immediate assistance.
Medical facilities using the Ingenia 1.5T MRI systems with the listed model numbers are most at risk. Patients undergoing MRI scans with these systems could experience treatment delays if the tabletop doesn't move properly during manual mode use.
Check if your MRI system has model numbers 781341 or 781396. The system's serial number (UDI#) is listed in the recall for specific units. This recall covers units sold in the U.S. with these model numbers.
Verify if your MRI system has model numbers 781341 or 781396.
No, the recall does not require immediate stop use. However, you should check if your system is affected by the model numbers listed.
Model numbers 781341 and 781396 are affected. The recall includes specific units with these model numbers and their serial numbers.
Check the model number on your MRI system. If it is 781341 or 781396, it is affected. The recall also lists specific serial numbers (UDI#) for affected units.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2411-2021 — Philips Philips Hello, I own a Philips that is covered by recall Z-2411-2021 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.
