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

Recall Z-1660-2023 — QUADROX -i Neonatal, Oxygenator used during cardiopulmonary bypass Model Item No. HMO 10000-USA 701070412 HMO 11000-USA 701070416

U.S. FDA — Device Enforcement · United States · 2023-05-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1660-2023
Date of alert
2023-05-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Maquet Medical Systems USA
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
701070412
Reported risk: Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis, and ischemia.
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.