Octopus Evolution AS Tissue Stabilizer — Class II medical device recall Z-2576-2026
Ongoing recall by Medtronic Perfusion Systems, reported 2026-07-01, distributed nationwide. During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorr
| Recall number | Z-2576-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Perfusion Systems, Brooklyn Park, MN, United States |
| Recall initiated | 2026-05-12 |
| Classified | 2026-06-24 |
| Reported by FDA | 2026-07-01 |
| Distributed | Nationwide (US) |
| Quantity | 288 units |
| UPC / GTIN / UDI-DI | 00613994764379, 00643169668904 |
| Serial numbers | 0232670681, 0232709164, 0232709168, 0232709194, 0232709199 |
| Model numbers | TS2500 |
Product
Octopus Evolution AS Tissue Stabilizer, Model TS2500
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2576-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.