Philips recalls Ingenia 1.5T CX-a MRI systems with potential delay in patient evacuation during manual mode use. Affected models include 781261 and 781262 with specific serial numbers. No remedy provided in official notice.
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 its Ingenia 1.5T CX-a MRI systems because the tabletop may not move completely in or out during manual mode, which could delay patient evacuation and treatment. This risk affects specific models with serial numbers listed in the recall notice.
When the MRI system is used in manual mode, the tabletop may not move fully in or out. This could prevent timely patient evacuation from the MRI bore, potentially delaying critical medical treatment.
Healthcare facilities using the Ingenia 1.5T CX-a MRI systems with serial numbers listed in the recall are affected. Patients undergoing scans with these systems may face delayed evacuation if the tabletop doesn't move properly during manual mode.
Check if your MRI system model is 781261 or 781262. Look for the specific serial numbers listed in the recall notice, which include a range of UDI numbers starting with 77000 through 77203.
Identify your MRI system model as either 781261 or 781262.
Confirm your system's serial number matches the list of UDI numbers provided in the recall notice.
The tabletop may not move completely in or out during manual mode, which could delay patient evacuation and treatment.
Models 781261 and 781262 with specific serial numbers listed in the recall notice.
The official recall notice does not provide a remedy.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2414-2021 — Philips Philips Hello, I own a Philips that is covered by recall Z-2414-2021 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.
