Public recall detail

Octopus Nuvo, Octopus Evo AS and Octopus 4

2026-05-13

medium
Cardiovascular Performance
Quick summary

Quick summary: Octopus Nuvo, Octopus Evo AS and Octopus 4. Reason: Performance. Category: Cardiovascular. Date: 2026-05-13.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Octopus Nuvo, Octopus Evo AS and Octopus 4. Reason: Performance. Category: Cardiovascular. Date: 2026-05-13.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandMEDTRONIC INC.
ProductOctopus Nuvo, Octopus Evo AS and Octopus 4
IssueMedical devices - Performance
Recall classType I
IdentificationRA-82070

Affected products

ProductOctopus Nuvo
Lot0231547054
ModelTSMICS1
Serial number0231547054
DescriptionOctopus Nuvo
ProductOctopus Nuvo
Lot0232670901
ModelTSMICS1
Serial number0232670901
DescriptionOctopus Nuvo
ProductOctopus Nuvo
Lot0232784925
ModelTSMICS1
Serial number0232784925
DescriptionOctopus Nuvo
ProductOctopus Nuvo
Lot0231912903
ModelTSMICS1
Serial number0231912903
DescriptionOctopus Nuvo
ProductOctopus Nuvo
Lot0231758880
ModelTSMICS1
Serial number0231758880
DescriptionOctopus Nuvo
ProductOctopus Nuvo
Lot0231792414
ModelTSMICS1
Serial number0231792414
DescriptionOctopus Nuvo
ProductOctopus Nuvo
Lot0231758898
ModelTSMICS1
Serial number0231758898
DescriptionOctopus Nuvo
ProductOctopus Evo AS
Lot0232709168
ModelTS2500
Serial number0232709168
DescriptionOctopus Evo AS
ProductOctopus 4
Lot0231478260
Model29400
Serial number0231478260
DescriptionOctopus 4
ProductOctopus 4
Lot0231468923
Model29400
Serial number0231468923
DescriptionOctopus 4

Issue

On 7-January-2026, Medtronic identified that the canister tubing set had been misassembled while performing final inspection. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, which is in reverse order than the design specification.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesMedtronic Inc. 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432
Recall date2026-05-12
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-82070
Background{}
CompaniesMedtronic Inc. 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432
AudiencesHealthcare
Source updated2026-05-13

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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