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Medium risk Medical DevicesClass II

CORFLO Safety PEG Kit ENFit Connector Recall

Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320

Updated April 30, 2026

Avanos Medical is recalling the CORFLO Safety PEG Kit with ENFit Connector (Model 50-4320) because some kits contain lidocaine hydrochloride injection with quality issues from a supplier recall. If you use this kit, stop and contact Avanos Medical before proceeding.

Is the Avanos Medical, Inc. recalled? Yes. This product was recalled by FDA on April 30, 2026. Details below.

What is recalled

CORFLO Safety PEG Kit with ENFit Connector, Model/Catalog Number 50-4320, manufactured by Avanos Medical, Inc.

Am I affected

You are affected if you have the CORFLO Safety PEG Kit with ENFit Connector, Model 50-4320. Check the model number on your kit packaging.

What to do right now

Stop using this kit immediately. Contact Avanos Medical for instructions on how to safely return or replace the affected product. Do not use the lidocaine hydrochloride injection that came with the kit.

The hazard

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

Brands affected

Avanos Medical, Inc.
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2337-2026
Classification
Class II
Recalled
April 30, 2026
Read the official notice

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