Philips recalls Ingenia 1.5T Evolution-a MRI systems where manual mode may cause tabletop movement delays, risking patient evacuation delays during procedures.
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 Evolution-a MRI systems because the tabletop might not move completely in or out during manual mode, which could delay patient evacuation from the MRI bore. This delay might impact timely treatment for patients.
When the tabletop doesn't move fully in or out during manual mode, it can cause delays in getting patients out of the MRI bore. This delay might prevent timely medical treatment, especially in emergencies.
Healthcare facilities using the recalled MRI systems are most at risk, particularly during patient procedures where quick evacuation is needed. Patients undergoing scans with these systems could face delayed treatment.
Check for model numbers 781315 or 78135 on the system. The serial numbers include specific UDI codes like 61019 (01)00884838099715 and others listed in the recall notice.
Look for model numbers 781315 or 78135 on the MRI system.
Check if the system has serial numbers starting with 61019 (01)00884838099715 or other specific UDI codes listed in the recall notice.
The tabletop may not move completely in or out during manual mode, which could delay patient evacuation from the MRI bore and impact timely treatment.
Check for model numbers 781315 or 78135 and serial numbers starting with specific UDI codes like 61019 (01)00884838099715 as listed in the recall notice.
No, but healthcare facilities should check if their system is affected and ensure proper operation to avoid delays in patient evacuation.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2412-2021 — Philips Philips Hello, I own a Philips that is covered by recall Z-2412-2021 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.
