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

Recall Z-1822-2020 — CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit

U.S. FDA — Device Enforcement · United States · 2020-03-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1822-2020
Date of alert
2020-03-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Avanos Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0203214820
Reported risk: The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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