Official recall record
Octopus Nuvo, Octopus Evo AS and Octopus 4
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-05-13
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
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 to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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