# FDA recall Z-1277-2018

> **Halyard Health, Inc** · Class II · device recall initiated 2017-12-13.

## Product

CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with Electromagnetic Transmitting Stylet and CORFLO* Enteral Feeding tube, ANTI-IV* Connector, 10 Fr, 140 cm    The device is used in patients that require intermittent or continuous tube feedings via the nasogastric or nasoenteric route.

## Reason for recall

The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI) Feeding Tubes with ANTI-IV* connector (Product Code 20-9551Trak2A) may be visible within the window of the exit port of the feeding tube.  Based on specifications, the transmitting stylet in the NG tube should not be visible within the port window.

## Distribution

Worldwide Distribution: US (nationwide) to states of: AR, CA, CO, GA, IA, LA, MI, MN, NM, TX; and country of Germany.      Distributed internationally to Germany.

## Key facts

- **Recall number:** Z-1277-2018
- **Recalling firm:** Halyard Health, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-13
- **Report date:** 2018-04-11
- **Termination date:** 2021-11-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Alpharetta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1277-2018

## Citation

> AI Analytics. FDA recall Z-1277-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1277-2018. Source: US FDA. Licensed CC0.

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