Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Recall Summary Avanos Medical is recalling MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) Kits, model 8180-20, distributed nationwide across all U.S. states and Washington D.C. The kits contain lidocaine hydrochloride injection that was recalled by its supplier due to quality issues. This is a Class II recall, meaning the product could cause serious health problems or failure, though it is not expected to cause death.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
- 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/e48ba822-50a2-4f97-a02c-a3a2a2591761