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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