Notice names this product. Medtronic Perfusion Systems’s Octopus Evolution Tissue Stabilizer is named in FDA Class II recall Z-2575-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: 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. Identifying details: UDI-DI: 00643169668911; Serial Numbers: 0232992409 0233010063 0233010115. Units affected: 134 units. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Octopus Evolution Tissue Stabilizer, Model TS2000
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
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 can…
Company / brand: Medtronic Perfusion Systems
Affected product: Octopus Evolution Tissue Stabilizer
Official ID Z-2575-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.