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

Recall Z-2106-2018 — Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 5909 14 Pack QPID, Part Number 701064992

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

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2106-2018
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)
3000018640
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.

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