Class II

Medical Device Recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500

Medtronic Perfusion Systems · May 12, 2026

Reason for Recall

During the manufacturing process, 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

Worldwide - US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

288 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2576-2026

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.

Medtronic Perfusion Systems Medical Device Recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500 | SafeCheck