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FDAClass II · Medical device · Recalled July 1, 2026
Octopus 4 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-2577-2026
- Brand
- Medtronic Perfusion Systems
- Classification
- Class II
- Units affected
- 590 units
- Recall status
- Ongoing
- Initiated
- Voluntary: Firm initiated
Description
Octopus 4 Tissue Stabilizer, Model 29400
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: 00763000543679; Serial Numbers: 0231266463 0231468923 0231478249 0231478253 0231478260 0231651627 0231651634 0231651636 0231651637 0231651638 0231651639 0231651641 0231651642
- 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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