GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph recall
GE Medical Systems Information Technologies Inc recalled GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph on August 12, 2026 because of software issue issue with the MAC VU360 v3.0 system. It was sold nationwide.
Why it was recalled
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's recalled
GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph
Quantity: 163 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- GE Medical Systems Information Technologies Inc, Milwaukee, WI
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Worldwide distribution - US Nationwide and the countries of Belgium, Hong Kong, Netherlands, Sweden, UK. - Status
- Ongoing
- Recall number
- Z-2876-2026
- Source
- U.S. Food and Drug Administration
More medical devices recalls
· Olympus Corporation of the AmericasMedline convenience kits containing Healthmark Instrument Channel Brushes
· Medline Industries, LPMidmark IQvitals Zone
· Midmark CorporationAchieva 3.0T; Model Numbers (REF)
· Philips North America LlcAutomated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1
· Abiomed, Inc.INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set
· CooperSurgical, Inc.