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Ge healthcare mac vu360, ref# part number 2030361-023; electrocardiograph

Official notice

12 Aug 2026

Last checked

22 Sept 2026

MediumFDA

An official FDA notice concerns GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2026-08-12. Recall numbers: Z-2876-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

163

Recall number

Z-2876-2026

Official notice

2026-08-12

The hazard

Health risk requiring medical assessment

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Event Ids

99400

Recall Numbers

Z-2876-2026

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Affected products

Product 1

GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph

Units affected

163

Risk / hazard

Health risk requiring medical assessment

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States

Affected area 1

US · United States

Affected area 2

BE · Belgium

Affected area 3

GB · United Kingdom

Affected area 4

HK · Hong Kong

Affected area 5

NL · Netherlands

Affected area 6

SE · Sweden

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: GE Medical Information. Contact: GE Medical Systems Information Technologies Inc.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-2876-2026

Event id

99400

Units affected

163

Status

active

Classification

Class II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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