Home/Recalls/FDA-Z-2335-2026
FDA DevicesClass II

Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312

Published: June 17, 2026Recall ID: Z-2335-2026Category: 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: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312

Affected Products

Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312

Additional Source Details

FieldValue
CityAlpharetta
StateGA
Event id98907
Address 15405 Windward Pkwy
Address 2N/A
Code infoLot Code: Model No 30-6312, UDI-DI 10350770007547, Lot Number 30365228
Postal code30004-4667
Report date20260617
Product typeDevices
Product quantity31 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