# FDA recall Z-2871-2017

> **Sorin Group USA, Inc.** · Class II · device recall initiated 2017-06-09.

## Product

Sorin Group Aortic Arch Cannula, 7 mm x 10 in x 3/8 in, Rx Only, Sterile    Product Usage:  The Aortic Arch Cannulae are indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

## Reason for recall

Identification of excess plastic on the tip of the cannula.

## Distribution

Worldwide Distribution - US Nationwide in the states of : AR, AZ, CA, GA, IL, IN, KS, MI, MN, MO, NC, NE, NY, OK, PA, SD, TX, & VA. and foreign countries of: Canada, Iran, Mexico, & New Zealand.

## Key facts

- **Recall number:** Z-2871-2017
- **Recalling firm:** Sorin Group USA, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-09
- **Report date:** 2017-08-16
- **Termination date:** 2023-11-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arvada, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2871-2017

## Citation

> AI Analytics. FDA recall Z-2871-2017. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-2871-2017. Source: US FDA. Licensed CC0.

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