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Medtronic Perfusion Systems recalls Octopus Evolution Tissue Stabilizer, Model TS2000
Recalled July 1, 2026 · FDA recall Z-2575-2026 · 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
134 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 Tissue Stabilizer, Model TS2000
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →