Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Recall Summary Avanos Medical is recalling CORFLO Safety PEG Kit (Model 30-5320), a gastrointestinal tube product distributed nationwide, because it contains lidocaine hydrochloride injection that was recalled by its supplier due to quality issues. This is a Class II recall affecting patients who may have received these kits.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320
- 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/0159329d-6ca0-4f7c-92f4-595113c6c562