# FDA recall Z-1822-2020

> **Avanos Medical, Inc.** · Class II · device recall initiated 2020-03-16.

## Product

CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit

## Reason for recall

The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted.

## Distribution

Worldwide and US Nationwide Distribution:  AZ, CA, CT, FL, GA, IA, ID, IL, LA, MO, MN, MD, NY, NM, NV, NJ, OR, OK, OH, RI, TN, TX, WA, WI,   ***Foreign:  Distributed to Australia, Belgium, Canada, France, Germany, Ireland, Italy, Netherlands, Romania, United Arab Emirates, United Kingdom

## Key facts

- **Recall number:** Z-1822-2020
- **Recalling firm:** Avanos Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-16
- **Report date:** 2020-05-06
- **Termination date:** 2023-08-31

- **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-1822-2020

## Citation

> AI Analytics. FDA recall Z-1822-2020. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1822-2020. Source: US FDA. Licensed CC0.

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