Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Recall Summary Avanos Medical is recalling CORFLO Safety PEG Kits (model 50-4320) distributed nationwide because they contain lidocaine hydrochloride injection that was recalled by the supplier due to quality issues. The kits are used for gastrointestinal feeding tubes and 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: 50-4320
- 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/07ae2a9b-59d5-48fb-a88b-b7947823ef05