# FDA recall Z-2480-2025

> **Medtronic Perfusion Systems** · Class I · device recall initiated 2025-08-06.

## Product

DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113 LV VENT 13FR, Model Number 12113

## Reason for recall

The catheters may not retain their shape.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-2480-2025
- **Recalling firm:** Medtronic Perfusion Systems
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-06
- **Report date:** 2025-09-10

- **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-2480-2025

## Citation

> AI Analytics. FDA recall Z-2480-2025. Retrieved 2026-07-25 from https://api.ai-analytics.org/recall/Z-2480-2025. Source: US FDA. Licensed CC0.

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