Home/Recalls/FDA-Z-2334-2026
FDA DevicesClass II

Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 3...

Published: June 17, 2026Recall ID: Z-2334-2026Category: 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

Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320

Affected Products

Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320

Additional Source Details

FieldValue
CityAlpharetta
StateGA
Event id98907
Address 15405 Windward Pkwy
Address 2N/A
Code infoUDI-DI 10350770007554, Lot Numbers 30365227, 30368642, 30374529, 30376099, 30380696, and 30387248
Postal code30004-4667
Report date20260617
Product typeDevices
Product quantity61 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