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Medtronic Perfusion Systems recalls Octopus Evolution AS Tissue Stabilizer, Model TS2500
Recalled July 1, 2026 · FDA recall Z-2576-2026 · Medtronic Perfusion Systems
Hazard
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. · FDA Class II
Units
288 units
Sold at
Worldwide - US Nationwide distribution.
Description
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.
Product
Octopus Evolution AS Tissue Stabilizer, Model TS2500
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →