Recall Ledger

Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number:... recall (Avanos Medical, Inc.)

Medical deviceClass IIOngoing

Summary: Avanos Medical, Inc. is recalling Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No. Reason: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

What is being recalled

Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No

Why

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

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution.

How to tell if yours is affected

UDI-DI 10350770007530, Lot Numbers 30365233, 30367015, 30372821, 30378386

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-2340-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedApril 30, 2026
ReportedJune 17, 2026
CompanyAvanos Medical, Inc.
Company locationAlpharetta, GA, United States
Initiated byVoluntary: Firm initiated
Quantity54 kits

More recalls from Avanos Medical, Inc. · all medical device recalls · recalls from April 2026

Official FDA record