Quick summary
Quick summary: CASE Cardiac Testing System - Parts. Reason: Performance. Category: Cardiovascular. Date: 2026-05-14.
Public recall detail
CASE Cardiac Testing System - Parts
2026-05-14
Cardiovascular
Performance
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: CASE Cardiac Testing System - Parts. Reason: Performance. Category: Cardiovascular. Date: 2026-05-14.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandGe Medical Systems Information Technologies Inc.
ProductCASE Cardiac Testing System - Parts
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82080
Affected products
ProductCASE Cardiac Testing System - Parts
LotMore than 10 numbers, contact manufacturer.
Model3031234-001
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionCASE Cardiac Testing System - Parts
Issue
Potential for electrical sparking at the printer head of CASE V7 systems.
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesGe Medical Systems Information Technologies Inc. 3114 N Grandview Blvd, Waukesha, Wisconsin, United States, 53188
Recall date2026-05-04
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82080
Background{}
CompaniesGe Medical Systems Information Technologies Inc. 3114 N Grandview Blvd, Waukesha, Wisconsin, United States, 53188
AudiencesHealthcare
Source updated2026-05-14
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
FAQ
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Product images
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