Recalling firm
Avanos Medical, Inc.
Product type
Device
Status
Ongoing
Report date
2026-06-17
Distribution
US Nationwide distribution.
Firm state
GA
Product quantity
3,184 kits
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental MonitoringReason for recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Product description
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20
Code / lot info
UDI-DI 10350770007783, Lot Numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, 80403340
Other recalls SPEQ maps to Environmental Monitoring
See all Environmental Monitoring recalls →Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.