Health product recall

Vivid Ultrasound Systems

Last updated

Summary

Product
Vivid Ultrasound Systems
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 catalogue number

Vivid S6 Ultrasound System - Main Unit

More than 10 numbers, contact manufacturer.

H45041QG
H45021WB
H45041FU
H45031TD
H45021LD

Vivid Q Ultrasound System - Cardiac & Vascular Application Modules

780407VQ1
902894VQ1
416586VQ1
780407VQ2
905668VQ1
514934BVQ1
905527VQ1
705743VQ1

H45021YC

Vivid I Ultrasound System

More than 10 numbers, contact manufacturer.

H45021A
H45031YW
H45041FL
H45021A/JK/AG

Vivid S5 Ultrasound System - Main Unit

More than 10 numbers, contact manufacturer.

H45021LC
H45041CS
H45041FP
H45041FS

Vivid Q Ultrasound System - Console

More than 10 numbers, contact manufacturer.

H45031YY
H45021WZ
H45031YZ
H45041FM

Vivid I Ultrasound System - Bt-09 Console

More than 10 numbers, contact manufacturer.

H45021WP

Vivid S6 Ultrasound System - Bt10 Console

More than 10 numbers, contact manufacturer.

H45031EC

Vivid I Ultrasound System - Software Options

519987VI
604631VIVID
204787VI1

H45041HH

Vivid S6 Ultrasound System - Software Options

519432VIV1
416691VS6A
416778VS6A
416422VS6

H45041JW

Vivid Q Ultrasound System - Software Options

604875VIVQ1

H45041HH

Issue

Potential for smoke or fire in certain legacy vivid ultrasound systems with batteries not replaced as recommended.

Recall start date: November 10, 2022

Additional information

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

Ge Medical Systems Israel Ltd.

Nativ Ha'Or Street No. 1, Haifa, Israel, 3508510

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-72221

Get notified

Receive notifications for new and updated recalls and alerts by category.

Subscribe