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

Recall Z-2104-2018 — Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET, Part Number 701054588

U.S. FDA — Device Enforcement · United States · 2016-03-11 · Class III

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2104-2018
Date of alert
2016-03-11
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Datascope Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
3000020069
Reported risk: There is a potential problem with the cuvette where failure of the cuvette would cause an error message on the monitor display of H/S DISCONNECT AT CUVETTE.
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.

Related

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.