# FDA recall Z-1032-2022

> **Avanos Medical, Inc.** · Class I · device recall initiated 2022-03-21.

## Product

Avanos Cortrak 2 Enteral Access System (EAS)

## Reason for recall

Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately.  CONFIRM placement of the NG/NI tube per institution protocol.

## Distribution

Worldwide Distribution. US Nationwide, Australia, Austria, Canada, Germany, Ireland, Kuwait, New Zealand, India, Japan, Malaysia, Netherlands, Panama, Singapore, Switzerland, and United Kingdom.

## Key facts

- **Recall number:** Z-1032-2022
- **Recalling firm:** Avanos Medical, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-03-21
- **Report date:** 2022-05-25
- **Termination date:** 2024-09-09

- **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-1032-2022

## Citation

> AI Analytics. FDA recall Z-1032-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1032-2022. Source: US FDA. Licensed CC0.

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