RecalledThisWeek Search
Medium risk Medical DevicesClass II

Avanos CORFLO Safety PEG Kit Recall

Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320

Updated April 30, 2026

Avanos Medical is recalling CORFLO Safety PEG kits with ENFit connectors because they contain lidocaine injection from a supplier with quality issues. This could affect the safety and sterility of the product.

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 50-5320, made by Avanos Medical, Inc.

Am I affected

You're affected if you have a CORFLO Safety PEG Kit with ENFit Connector, Model 50-5320 from Avanos Medical in your possession or use.

What to do right now

Stop using this product immediately. Contact Avanos Medical or your healthcare provider for instructions on return or replacement.

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-2338-2026
Classification
Class II
Recalled
April 30, 2026
Read the official notice

Get free recall alerts

New Medical Devices recalls, the moment they post.

Free forever. Unsubscribe anytime. We never sell your data.

More Medical Devices recalls