Health product recall

Venue Fit and Venue Go

Last updated

Summary

Product
Venue Fit and Venue Go
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Venue Fit

More than 10 numbers, contact manufacturer.

VENUE FIT R4
VENUE FIT R3

Venue Go

More than 10 numbers, contact manufacturer.

VENUE GO R4
VENUE GO R2
VENUE GO R3

Issue

GE Healthcare has become aware that the battery for certain Venue Go and Venue Fit ultrasound systems with software versions R2, R3, and R4 can potentially develop an internal failure which could result in smoke or fire.

Recall Start Date: March 17, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Physical medicine
Companies

Ge Medical Systems Ultrasound & Primary Care Diagnostics Llc

3200 N Grandview Blvd, Waukesha, Wisconsin, United States, 53188

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77185

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