Fresh Recalls

FDAClass II · Medical device · Recall Z-2576-2026 · Recalled July 1, 2026

Octopus Evolution AS Tissue Stabilizer recall — Medtronic Perfusion Systems

Agency report date: July 1, 2026.

1. Compare your item

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.

Product named
Octopus Evolution AS Tissue Stabilizer
Company / brand
Medtronic Perfusion Systems
Lot / serial / date codes
UDI-DI: 00643169668904, 00613994764379; Serial Numbers: 0232670681 0232709164 0232709168 0232709194 0232709194 0232709199
Distribution
Worldwide - US Nationwide distribution.
Agency product description and boundaries

Octopus Evolution AS Tissue Stabilizer, Model TS2500

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.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

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

Affected product: Octopus Evolution AS Tissue Stabilizer

3. Open the official notice or contact

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

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
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

Report a data error on this page