# FDA recall Z-3128-2024

> **Medtronic Perfusion Systems** · Class II · device recall initiated 2024-07-09.

## Product

Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312

## Reason for recall

During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).

## Distribution

Worldwide distribution - US Nationwide and the countries of Cambodia, Greece, Ireland, Italy, Saudi Arabia, Switzerland, United Kingdom, Viet Nam.

## Key facts

- **Recall number:** Z-3128-2024
- **Recalling firm:** Medtronic Perfusion Systems
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-09
- **Report date:** 2024-09-18

- **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-3128-2024

## Citation

> AI Analytics. FDA recall Z-3128-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-3128-2024. Source: US FDA. Licensed CC0.

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