Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
CORFLO® Safety PEG Kit Recall Summary Avanos Medical is recalling CORFLO® Safety PEG Kit (Model 30-6312), a gastrointestinal tube kit distributed nationwide, because it contains lidocaine hydrochloride injection that was recalled by its supplier due to quality issues. The recall affects kits distributed across all U.S. states and Washington D.C.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
- 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/4959ff55-0355-4824-850d-810b9a496a08