Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Recall Summary Avanos Medical is recalling CORFLO Safety PEG Kits with ENFit Connector (Model 50-5320) distributed nationwide because the kits contain lidocaine hydrochloride injection that was recalled by the supplier due to quality issues. This is a Class II recall affecting medical facilities and patients who use these gastrointestinal tubes and kits across all U.S. states.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Product Name: CORFLO* Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-5320
- Reason
- Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-30
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/642c284e-4ebe-4402-b024-8de2fe549c91