Reported Jul 1, 2026 · Ongoing · Updated Sep 16, 2026
Octopus Evolution Tissue Stabilizer, Model TS2000
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 Tissue Stabilizer, Model TS2000
- Lot codes and dates
- UDI-DI00643169668911
- Serial Numbers0232992409 0233010063 0233010115
- Amount recalled
- 134 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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