# FDA recall Z-2766-2017

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

## Product

DLP Cardioplegia Adapter with Pressure Port  Provides access for a pressure monitoring needle near the connection to the cardioplegia cannula. These adapters are intended for use in conjunction with the delivery of cardioplegia solution and to provide access for pressure monitoring for up to six hours

## 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-2766-2017
- **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-2766-2017

## Citation

> AI Analytics. FDA recall Z-2766-2017. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-2766-2017. Source: US FDA. Licensed CC0.

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