Home/Recalls/FDA-Z-2342-2026
FDA DevicesClass II

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUS...

Published: June 17, 2026Recall ID: Z-2342-2026Category: 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 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No

Affected Products

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No

Additional Source Details

FieldValue
CityAlpharetta
StateGA
Event id98907
Address 15405 Windward Pkwy
Address 2N/A
Code infoLot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746
Postal code30004-4667
Report date20260617
Product typeDevices
Product quantity901 kits
Reason for recallLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260430
Initial firm notificationN/A
Center classification date20260605

Overview

  • Recalling FirmAvanos Medical, Inc.
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution.
Official Agency Alert