Recall Monitor
Health ProductsType I recall

Octopus Nuvo, Octopus Evo AS and Octopus 4

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - Cardiovascular
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
Recall class: Type I
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Products

Affected productsLot or serial numberModel or catalogue number
Octopus Nuvo0231547054TSMICS1
Octopus Nuvo0232670901TSMICS1
Octopus Nuvo0232784925TSMICS1
Octopus Nuvo0231912903TSMICS1
Octopus Nuvo0231758880TSMICS1
Octopus Nuvo0231792414TSMICS1
Octopus Nuvo0231758898TSMICS1
Octopus Evo AS0232709168TS2500
Octopus 4023147826029400
Octopus 4023146892329400

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.

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