Octopus Evolution Tissue Stabilizer recall
Octopus Evolution Tissue Stabilizer, Model TS2000
Why was Octopus Evolution Tissue Stabilizer 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 00643169668911; Serial Numbers: 0232992409 0233010063 0233010115
- Product
- Octopus Evolution Tissue Stabilizer, Model TS2000
- Recalling firm
- Medtronic Perfusion Systems
- Quantity
- 134 units
- Distribution
- Worldwide - US Nationwide distribution.
- Recall date
- July 1, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)