Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Recall Summary Avanos Medical is recalling MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) feeding tube kits (Model 8170-14, 14 Fr) because they contain lidocaine hydrochloride injection that was recalled by the supplier due to quality issues. The affected kits were distributed nationwide across all U.S. states. This is classified as a Class II recall, meaning the product could cause temporary or reversible health problems.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No
- 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/2d431949-84f9-444f-9b3d-5824cec95ac0