GE recalls Vivid E90 and E95 ultrasound systems with model numbers H45581LB and H45581DA due to potential display of wrong patient names and demographics on scans.
GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner screen rather than the intended patient selected by the user.
GE is recalling Vivid E90 and E95 ultrasound systems because they may show incorrect patient names and demographics on the screen. This could lead to misdiagnosis if the wrong patient's information is used during scans.
The ultrasound systems may display incorrect patient names and demographics due to a slow DICOM Worklist response time. This could result in the wrong patient's information being used during scans, potentially causing misdiagnosis.
Healthcare providers using GE Vivid E90 or E95 ultrasound systems with specific model numbers and serial numbers are affected. Patients undergoing scans with these systems may be at risk of misdiagnosis.
Check for model numbers H45581LB (Vivid E90) or H45581DA (Vivid E95) with serial numbers AU01170, AU01180, AU50159 or AU01095, AU50476, AU50252, AU01002.
Verify your ultrasound system's model number is H45581LB for Vivid E90 or H45581DA for Vivid E95.
Check if your system has serial numbers AU01170, AU01180, AU50159 or AU01095, AU50476, AU50252, AU01002.
GE HealthCare has identified that certain Vivid ultrasound systems may display incorrect patient names and demographics due to a slow DICOM Worklist response time.
The system might show the wrong patient's information during scans, which could lead to misdiagnosis if not corrected.
Check for model numbers H45581LB (Vivid E90) or H45581DA (Vivid E95) with serial numbers AU01170, AU01180, AU50159 or AU01095, AU50476, AU50252, AU01002.
We’ve drafted a message you can send GE Vingmed to request your refund or repair — edit it as you like.
Subject: Recall Z-2316-2024 — GE Vingmed GE Vingmed Hello, I own a GE Vingmed that is covered by recall Z-2316-2024 from GE Vingmed. 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.
