# FDA recall Z-2765-2017

> **Medtronic Perfusion Systems** · Class II · device recall initiated 2017-06-22.

## Product

DLP Antegrade/Retrograde Adapter  Method for perfusion of cardioplegia alternately in either an antegrade or retrograde fashion. It is fitted with flexible lines and standard luer sites to facilitate direct connections to the cannulae

## Reason for recall

Identification of small pinholes in a single packaging configuration of sterile pouches.  A total of seven different products were affected.

## Distribution

Worldwide Distribution - US (nationwide) Foreign: Argentina, Australia, Austria, Belgium, Bulgaria, Canada, Croatia, Denmark, El Salvador, France, Georgia, Germany, Hungary, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Macedonia, Moldova, Netherlands, New Zealand, Nigeria, Norway, Poland, Romania, Russian Federation, Slovenia, Spain, Thailand, Turkey, & United Kingdom.

## Key facts

- **Recall number:** Z-2765-2017
- **Recalling firm:** Medtronic Perfusion Systems
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-22
- **Report date:** 2017-08-02
- **Termination date:** 2020-07-22

- **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-2765-2017

## Citation

> AI Analytics. FDA recall Z-2765-2017. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2765-2017. Source: US FDA. Licensed CC0.

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