# FDA recall Z-0371-2020

> **Avanos Medical, Inc.** · Class II · device recall initiated 2019-10-08.

## Product

CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit with ENFit Connector.  2 units per case    The devices could be branded as Halyard Health.

## Reason for recall

The connector piece to the PEG tube does not pass over the guidewire.

## Distribution

Distribution to CT, IN, MD, NJ, PA, VA.      International distribution to Great Britain.

## Key facts

- **Recall number:** Z-0371-2020
- **Recalling firm:** Avanos Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-08
- **Report date:** 2019-11-20
- **Termination date:** 2022-03-16

- **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-0371-2020

## Citation

> AI Analytics. FDA recall Z-0371-2020. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0371-2020. Source: US FDA. Licensed CC0.

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