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
Get notified
Receive emails about new and updated recall and safety alerts.