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 FIT R5 |
| Venue Go | More than 10 numbers, contact manufacturer. | VENUE GO R4 VENUE GO R2 VENUE GO R3 VENUE GO R5 |
Issue
GE Healthcare has become aware that the battery for certain Venue Go and Venue Fit ultrasound systems with software versions R2, R3, R4, and R5 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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