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