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

Recall Z-0489-2024 — vyaire Flexible Patient Circuit, 3100A, REF 29028-004, intended to be used with the 3100A High Frequency Oscillatory Ventilator (HFOV)

U.S. FDA — Device Enforcement · United States · 2023-10-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0489-2024
Date of alert
2023-10-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Vyaire Medical
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10190752155251
Reported risk: Two patient circuits, 29028-003 and 29028-004, for the 3100 High Frequency Oscillatory ventilator that are only approved for use outside the U.S. were distributed in the U.S.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.