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Limited official informationFDA Medical Device Enforcement ReportsRecall date: Jul 1, 2026

Octopus Evolution AS Tissue Stabilizer, Model TS2500

Full official product description

Octopus Evolution AS Tissue Stabilizer, Model TS2500 | Octopus 4 Tissue Stabilizer, Model 29400 | Octopus Evolution Tissue Stabilizer, Model TS2000

Verification delayed

The last verified facts remain visible. Last successful verification: Aug 5, 2026, 7:44 AM UTC. A temporary source failure does not mean the recall changed.

Official information is incomplete

Missing: action, consumer scope. The page is public for lookup but excluded from search indexing and advertising.

1Is my item affected?

Compare the complete identifiers. Name similarity alone is not a confirmed match.

Octopus Evolution AS Tissue Stabilizer, Model TS2500; Octopus 4 Tissue Stabilizer, Model 29400; plus 1 additional official variants listed below.

Identifiers to compare

  • UDI 00643169668904
  • UDI 00763000543679
  • UDI 00643169668911
  • Model TS2500
  • Model 29400
  • Model TS2000
  • Serial Numbers
Affected variants from the official event record
Product or modelCodes and lotsQuantityRecall number
Octopus Evolution AS Tissue Stabilizer, Model TS2500UDI-DI: 00643169668904, 00613994764379; Serial Numbers: 0232670681 0232709164 0232709168 0232709194 0232709194 0232709199288 unitsZ-2576-2026
Octopus 4 Tissue Stabilizer, Model 29400UDI-DI: 00763000543679; Serial Numbers: 0231266463 0231468923 0231478249 0231478253 0231478260 0231651627 0231651634 0231651636 0231651637 0231651638 0231651639 0231651641 0231651642590 unitsZ-2577-2026
Octopus Evolution Tissue Stabilizer, Model TS2000UDI-DI: 00643169668911; Serial Numbers: 0232992409 0233010063 0233010115134 unitsZ-2575-2026

2What is the risk?

The agency's statement is shown without a site-authored severity score.

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.

Agency classification: Class II

3What should I do?

Only instructions associated with this recall event qualify as an action.

Consumer action is not available in the associated official record. The site does not infer or generate a replacement.

Verify on the official source

The linked agency record controls if any information differs.

Official evidence

Official scope

Distribution reported by the agency

Worldwide - US Nationwide distribution.

Distribution is context, not a confirmed item match. Compare the model, lot, UPC, NDC, or serial number above.

Material change history

No material affected-item, risk, action, or status change has been recorded since this page entered the tracker.