Reported Jul 1, 2026 · Ongoing · Updated Sep 16, 2026
Octopus Evolution AS Tissue Stabilizer, Model TS2500
Medtronic Perfusion Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Perfusion Systems · 7611 Northland Dr N · Brooklyn Park, MN · 55428-1088
Is this the product you have?
- Octopus Evolution AS Tissue Stabilizer, Model TS2500
- Lot codes and dates
- UDI-DI
0064316966890400613994764379
- Serial Numbers0232670681 0232709164 0232709168 0232709194 0232709194 0232709199
- UDI-DI
- Amount recalled
- 288 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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