Medtronic recalls Octopus Evolution Tissue Stabilizer Model TS2000 with incorrect tube assembly. Affected units have serial numbers 0232992409, 0233010063, 0233010115. No remedy provided in recall notice.
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.
Medtronic is recalling specific Octopus Evolution Tissue Stabilizer models due to incorrect tube assembly during manufacturing. This could lead to improper function but does not pose an immediate safety risk.
The tubing was attached incorrectly during manufacturing, with the short tube on the bottom and long tube on the top instead of the intended design. This could cause improper fluid flow or device function but does not involve immediate safety hazards like injury or fire.
Users of the Octopus Evolution Tissue Stabilizer Model TS2000 with serial numbers 0232992409, 0233010063, or 0233010115 are affected. Medical professionals using this device for tissue stabilization are most at risk.
Check for the Octopus Evolution Tissue Stabilizer Model TS2000 with serial numbers 0232992409, 0233010063, or 0233010115. The UDI-DI code 00643169668911 may also help identify affected units.
Verify if your device has serial numbers 0232992409, 0233010063, or 0233010115.
The recall notice does not provide a remedy for this issue.
Check for the serial numbers 0232992409, 0233010063, or 0233010115 on your Octopus Evolution Tissue Stabilizer Model TS2000.
The recall notice does not specify any action to take for affected units.
We’ve drafted a message you can send Medtronic Perfusion Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2575-2026 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-2575-2026 from Medtronic Perfusion Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
