GE Vingmed Ultrasound As 2024-07-17 Health serious FDA
Health · FDA · Recall #FDA-Z-2317-2024
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW Recall
Issued July 17, 2024 · GE Vingmed Ultrasound As
In July 2024, GE Vingmed Ultrasound As recalled the GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact GE Vingmed Ultrasound As to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- GE Vingmed Ultrasound As
- Category
- Health
- Recall date
- July 17, 2024
- Units affected
- Not reported
- Sold at
- US: IL, MA, NM, NY, OK,
- Recall number
- FDA-Z-2317-2024
- Made in
- Norway
- Issuing agency
- FDA
In context
- GE Vingmed Ultrasound As has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.