Avanos Medical, Inc.: Tubes, Gastrointestinal (and Accessories)
Avanos Medical is recalling MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kits (model 8170-24) distributed nationwide because they contain lidocaine 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, which means the product could cause adverse health effects or serious problems.
- Recalling firm
- Avanos Medical, Inc.
- Product
- Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24
- 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/73dc8dd8-6268-406e-9449-5fa6bd874785