Health product recall

Vivid Ultrasound Systems

Last updated

Summary

Product
Vivid Ultrasound Systems
Issue
Medical devices - Performance issue
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

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