GE Medical Systems Information Technologies Inc 2026-08-12 Health serious FDA
Health · FDA · Recall #FDA-Z-2876-2026
GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph Recall
Issued August 12, 2026 · GE Medical Systems Information Technologies Inc
In August 2026, GE Medical Systems Information Technologies Inc recalled the GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph, a serious health recall reported by the FDA.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of inactivity. As a result, data from a previous patient may remain on the screen and could be incorrectly associated with a subsequent patient.
What you should do
- 1 Stop using GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact GE Medical Systems Information Technologies Inc 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 Medical Systems Information Technologies Inc
- Category
- Health
- Recall date
- August 12, 2026
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Belgium, Hong Kong, Netherlands, Sweden, UK.
- Recall number
- FDA-Z-2876-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- GE Medical Systems Information Technologies Inc has 2 recalls in our database.
- We're tracking 3,707 Health recalls in our database.
- This is the 487th Health recall we've logged in 2026.