Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Recall Summary Avanos Medical is recalling CORFLO Safety PEG Kits with ENFit Connector (model 50-6312) distributed nationwide because they contain lidocaine hydrochloride injection that was recalled by the supplier due to quality issues. This is a Class II recall affecting gastrointestinal tubes and accessories that were distributed across all U.S. states and Washington, D.C.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Product Name: CORFLO* Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6312
- 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/f802e0cd-bfe1-4c8b-a536-c5e9fa9c9f65