Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit Recalled by Avanos Medical, Inc. Due to The connector piece to the PEG tube does...

Date: October 8, 2019
Company: Avanos Medical, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Avanos Medical, Inc. directly.

Affected Products

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

Quantity: 104 cases (208 units) total

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 6 states: CT, IN, MD, NJ, PA, VA

Affected (6 states)Not affected

About Avanos Medical, Inc.

Avanos Medical, Inc. has 37 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report