Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0565-2022 — MIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL

U.S. FDA — Device Enforcement · United States · 2021-12-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0565-2022
Date of alert
2021-12-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Avanos Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
30116959
Reported risk: The External Retention Bolster contained in the kit may be a larger diameter than the tube.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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