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

Recall Z-1309-2024 — NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: (1) 48145; (2) 48145E

U.S. FDA — Device Enforcement · United States · 2023-10-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1309-2024
Date of alert
2023-10-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Mc3 Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10854916006888
Reported risk: May have increased water path restriction within the heat exchanger, leading to degraded heat exchange performance during use. The reduction of water flow and reduced heat exchange performance may be experienced immediately upon priming or may worsen over the duration of use. The potential harm as stated in the IFU includes hypothermia due to inadequate heat transfer
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.