# FDA recall Z-2333-2026

> **Avanos Medical, Inc.** · Class II · device recall initiated 2026-04-30.

## Product

Brand Name: CORFLO  Product Name: CORFLO* Safety PEG Kit  Model/Catalog Number: 30-4320

## Reason for recall

Lidocaine hydrochloride injection, the subject of a supplier recall for  quality issues, were included into sterile kits and sets.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2333-2026
- **Recalling firm:** Avanos Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-30
- **Report date:** 2026-06-17

- **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-2333-2026

## Citation

> MORVS. FDA recall Z-2333-2026. Retrieved 2026-10-14 from https://api.morvs.ai/recall/Z-2333-2026. Source: US FDA. Licensed CC0.

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