Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Recall Summary Avanos Medical is recalling MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) Kits with ENFit Connectors (model 8180-14) distributed nationwide because they contain lidocaine hydrochloride injections that were recalled by the supplier due to quality issues. The kits were distributed across all U.S. states and the District of Columbia. This is a Class II recall, meaning the product could cause serious health problems or death.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14
- 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/a48a2d2f-77a0-4987-8d30-77aae9b10077