Home/Recalls/FDA-Z-2344-2026
FDA DevicesClass II

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUL...

Published: June 17, 2026Recall ID: Z-2344-2026Category: 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 14 Fr PULL Model/Catalog Number: 7180-14

Affected Products

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14

Additional Source Details

FieldValue
CityAlpharetta
StateGA
Event id98907
Address 15405 Windward Pkwy
Address 2N/A
Code infoUDI-DI 10350770007769, Lot Numbers 30371312 and 30373421
Postal code30004-4667
Report date20260617
Product typeDevices
Product quantity208 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