FDA DevicesClass II
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUL...
Published: June 17, 2026Recall ID: Z-2346-2026Category: devicesCountry: US
Reason for Recall / Hazard
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Product Description & Identification
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
Affected Products
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
Additional Source Details
| Field | Value |
|---|---|
| City | Alpharetta |
| State | GA |
| Event id | 98907 |
| Address 1 | 5405 Windward Pkwy |
| Address 2 | N/A |
| Code info | UDI-DI 10350770007806, Lot Numbers 30371316, 30377829, 80403341 |
| Postal code | 30004-4667 |
| Report date | 20260617 |
| Product type | Devices |
| Product quantity | 1,006 kits |
| Reason for recall | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260430 |
| Initial firm notification | N/A |
| Center classification date | 20260605 |
Overview
- Recalling FirmAvanos Medical, Inc.
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution.