# FDA recall Z-2767-2017

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

## Product

DLP Pressure Monitoring Extension Line Adapters  Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.

## 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-2767-2017
- **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-2767-2017

## Citation

> AI Analytics. FDA recall Z-2767-2017. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-2767-2017. Source: US FDA. Licensed CC0.

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