Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIOngoing
Summary: Avanos Medical, Inc. is recalling Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24. Reason: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
What is being recalled
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24
Why
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution.
How to tell if yours is affected
UDI-DI 10350770007868, Lot Numbers 30371319, 30374055, 30383058, 30386936
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2352-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | April 30, 2026 |
| Reported | June 17, 2026 |
| Company | Avanos Medical, Inc. |
| Company location | Alpharetta, GA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 1,205 kits |
More recalls from Avanos Medical, Inc. · all medical device recalls · recalls from April 2026