# FDA recall Z-1801-2024

> **Medtronic Perfusion Systems** · Class II · device recall initiated 2024-03-19.

## Product

Medtronic Cardioplegia Adapters:    a) DLP¿ 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter, Model Number 25009,   b) DLP¿ 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter, Model Number 25010,   c) DLP¿ 30.5 cm (12 in) Multiple Perfusion Set, Model Number 14003,   d) DLP¿ 38.1 cm (15 in) Multiple Perfusion Set, Model Number 14000,   e) DLP¿ 50.8 cm (20 in) Extension Line Adapter, Model Number 11001G,   f) DLP¿ Perfusion/Venting Adapter, Model Number 13002,   g) DLP¿  Y  Adapter   Coronary Perfusion, Model Number 10710

## Reason for recall

Potential for unsealed sterile packing.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1801-2024
- **Recalling firm:** Medtronic Perfusion Systems
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-19
- **Report date:** 2024-05-22

- **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-1801-2024

## Citation

> AI Analytics. FDA recall Z-1801-2024. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-1801-2024. Source: US FDA. Licensed CC0.

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