Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Recall Summary Avanos Medical is recalling CORFLO Safety PEG Kits (Model 30-4320) distributed nationwide because they contain lidocaine hydrochloride injection that was recalled by the supplier due to quality issues. These are sterile medical kits used for gastrointestinal tubes and related procedures. The recall affects products distributed across all U.S. states.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320
- 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/c080e42e-542b-45a8-a127-6986acdf55f6