FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass II · Medical device · Recalled July 1, 2026

Octopus Evolution AS Tissue Stabilizer recall — Medtronic Perfusion Systems

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.

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
Z-2576-2026
Brand
Medtronic Perfusion Systems
Classification
Class II
Units affected
288 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

Octopus Evolution AS Tissue Stabilizer, Model TS2500

Affected products

Companies & origin

Recalling firm location
Brooklyn Park, MN, United States
Firm address
7611 Northland Dr N, N/A, 55428-1088

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI: 00643169668904, 00613994764379; Serial Numbers: 0232670681 0232709164 0232709168 0232709194 0232709194 0232709199
Distribution
Worldwide - US Nationwide distribution.
Firm notified the public via
Letter
FDA event ID
98966
Recall initiated
May 12, 2026
FDA classified
June 24, 2026
FDA report date
July 1, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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