Class II

Medical Device Recall: Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1

Medtronic Perfusion Systems · January 13, 2026

Reason for Recall

During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

Distribution

US Nationwide distribution in the states of FL and IN.

States Affected

NATIONWIDE

Quantity Affected

2 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1473-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.