# FDA recall Z-1473-2026

> **Medtronic Perfusion Systems** · Class II · device recall initiated 2026-01-13.

## Product

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

## Reason for recall

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.

## Distribution

US Nationwide distribution in the states of FL and IN.

## Key facts

- **Recall number:** Z-1473-2026
- **Recalling firm:** Medtronic Perfusion Systems
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-13
- **Report date:** 2026-03-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brooklyn Park, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1473-2026

## Citation

> AI Analytics. FDA recall Z-1473-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1473-2026. Source: US FDA. Licensed CC0.

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