Medtronic Perfusion Systems recalls Octopus Evolution Tissue Stabilizer
- Recalling company
- Medtronic Perfusion Systems
- Product
- Octopus Evolution Tissue Stabilizer, Model TS2000
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 12, 2026
- Reported
- Jul 1, 2026
- Distribution
- Worldwide - US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 134 units
- Lot / codes
- UDI-DI: 00643169668911; Serial Numbers: 0232992409 0233010063 0233010115
- Company location
- Brooklyn Park, MN
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2575-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2575-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.