Health product recall

Octopus Nuvo, Octopus Evo AS and Octopus 4

Brand(s)
Last updated

Summary

Product
Octopus Nuvo, Octopus Evo AS and Octopus 4
Issue
Medical devices - Performance
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

Octopus Nuvo

0231547054

TSMICS1

Octopus Nuvo

0232670901

TSMICS1

Octopus Nuvo

0232784925

TSMICS1

Octopus Nuvo

0231912903

TSMICS1

Octopus Nuvo

0231758880

TSMICS1

Octopus Nuvo

0231792414

TSMICS1

Octopus Nuvo

0231758898

TSMICS1

Octopus Evo AS

0232709168

TS2500

Octopus 4

0231478260

29400

Octopus 4

0231468923

29400

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.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Medtronic Inc.
710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Recall date
Identification number
RA-82070

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