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

Recall Z-1576-2019 — Maquet Getinge-BEQ-T 16405 LIVER TX INFUSION Material:701066097

U.S. FDA — Device Enforcement · United States · 2019-04-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1576-2019
Date of alert
2019-04-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Maquet Cardiovascular, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
3000055324
Reported risk: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During sterilization, the closed stopcock/non-vented cap configuration may prevent the flow of humidity/ethylene oxide gas into the fluid-path between the closed port and the non-vented cap therefore the Sterility Assurance Level (SAL) of the stopcock ports cannot be assured
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.