Recall Ledger

Octopus Nuvo Tissue Stabilizer recall (Medtronic Perfusion Systems)

Medical deviceClass IIOngoing

Summary: Medtronic Perfusion Systems is recalling Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1. Reason: During the manufacturing, 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.

What is being recalled

Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1

Why

During the manufacturing, 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.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide. Global Distribution.

How to tell if yours is affected

UDI-DI: 00763000543693; Lot Number: 0232837110, Additional lots as of 5/22/26: 0231547054 0231591827 0231758880 0231758898 0231758932 0231792414 0231792421 0231912903 0232670901 0232709219 0232709254 0232744928 0232784925 0232784989 0232805458

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-1473-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedJanuary 13, 2026
ReportedMarch 4, 2026
CompanyMedtronic Perfusion Systems
Company locationBrooklyn Park, MN, United States
Initiated byVoluntary: Firm initiated
Quantity939 units

More recalls from Medtronic Perfusion Systems · all medical device recalls · recalls from January 2026

Official FDA record