Quick summary
Quick summary: Vivo 45 LS. Reason: Performance. Category: Anaesthesiology. Date: 2026-05-01.
Public recall detail
Vivo 45 LS
2026-05-01
Anaesthesiology
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: Vivo 45 LS. Reason: Performance. Category: Anaesthesiology. Date: 2026-05-01.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandBreas Medical Ab
ProductVivo 45 LS
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82020
Affected products
ProductVivo 45 LS
LotS/N: 1R070KF to 1R100F9
Model230000
Serial numberS/N: 1R070KF to 1R100F9
DescriptionVivo 45 LS
Issue
In devices with the affected firmware versions, treatment in volume-controlled ventilation modes (VCV, VCV-SIMV and VCV-MPV) can, under specific trigger conditions, result in delivered tidal volume being reduced significantly below the set value.
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Anaesthesiology
CompaniesBreas Medical AB Foretagsvagen 1, Molnlycke, Sweden, 43533
Recall date2026-04-17
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82020
Background{}
CompaniesBreas Medical AB Foretagsvagen 1, Molnlycke, Sweden, 43533
AudiencesHealthcare
Source updated2026-05-01
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
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