Quick summary
Quick summary: Horizon Medical Imaging System. Reason: Health product recall. Category: Health products. Date: 2026-11-05.
Public recall detail
Horizon Medical Imaging System
2026-11-05
Health products
Health product recall
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Horizon Medical Imaging System. Reason: Health product recall. Category: Health products. Date: 2026-11-05.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandHologic, Inc.
ProductHorizon Medical Imaging System
IssueMedical devices - Device compatibility
Recall classType II
IdentificationRA-82912
Affected products
ProductHorizon Medical Imaging System
Lot309700M
ModelHORIZON WI
Serial number309700M
DescriptionHorizon Medical Imaging System
ProductHorizon Medical Imaging System
Lot309701M
ModelHORIZON WI
Serial number309701M
DescriptionHorizon Medical Imaging System
ProductHorizon Medical Imaging System
Lot309702M
ModelHORIZON WI
Serial number309702M
DescriptionHorizon Medical Imaging System
ProductHorizon Medical Imaging System
Lot309700M
ModelHORIZON W
Serial number309700M
DescriptionHorizon Medical Imaging System
ProductHorizon Medical Imaging System
Lot309701M
ModelHORIZON W
Serial number309701M
DescriptionHorizon Medical Imaging System
ProductHorizon Medical Imaging System
Lot309702M
ModelHORIZON W
Serial number309702M
DescriptionHorizon Medical Imaging System
Issue
It was identified that certain replacement monitors for Horizon W/WI systems released into production beginning in January 2025 were shipped without the VGA cable required to connect the monitor to the computer. As a result, field service engineers may have installed the systems using VGA cables from unknown origin. This created a nonconformance related to the use of unapproved components and a potential risk of increased electromagnetic interference (EMI) emissions from VGA cables that have not been evaluated or approved by Hologic.
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Radiology
CompaniesHologic, Inc. 600 Technology Drive, Newark, Delaware, United States, 19702
Recall date2026-09-28
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82912
Original published date2026-11-05
Background{}
CompaniesHologic, Inc. 600 Technology Drive, Newark, Delaware, United States, 19702
AudiencesHealthcare
Source updated2026-11-05
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
FAQ
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