FDAClass IIJune 17, 2026

MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recall

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24

Why was MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit recalled?

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI 10350770007868, Lot Numbers 30371319, 30374055, 30383058, 30386936

Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24
Recalling firm
Avanos Medical, Inc.
Quantity
1,205 kits
Distribution
US Nationwide distribution.
Recall date
June 17, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls