Medtronic recalls Octopus Evolution AS Tissue Stabilizer Model TS2500 with incorrect tube assembly. Affected units have specific serial numbers and UDI-DI codes. Consumers should contact Medtronic for details.
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 Octopus Evolution AS Tissue Stabilizer Model TS2500 due to incorrect tube assembly during manufacturing. This could lead to improper function of the device if used as intended.
The tubing was incorrectly attached to the canister during manufacturing, with the short tube on the bottom and long tube on the top instead of the intended design. This could cause improper function of the device but does not pose an immediate safety risk.
Users of the Octopus Evolution AS Tissue Stabilizer Model TS2500 are affected. Those with the specific serial numbers or UDI-DI codes listed are most at risk.
Check for the specific serial numbers: 0232670681, 0232709164, 0232709168, 0232709194, 0232709199. Also look for UDI-DI codes: 00643169668904 and 00613994764379.
Verify your Octopus Evolution AS Tissue Stabilizer Model TS2500 has the specific serial numbers or UDI-DI codes listed in the recall notice.
Medtronic is recalling Octopus Evolution AS Tissue Stabilizer Model TS2500 due to incorrect tube assembly during manufacturing.
Check for the specific serial numbers: 0232670681, 0232709164, 0232709168, 0232709194, 0232709199 or UDI-DI codes: 00643169668904, 00613994764379.
The recall does not specify a remedy, so contact Medtronic directly for further instructions.
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-2576-2026 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-2576-2026 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.
