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

Recall Z-0835-2013 — VACUETTE Safety Blood Collection Set + Luer Adapter, 23x12" Safety Blood Collect LA Product, Item number 450096. Usage: The Safety Blood Collection Set is used in routine venipuncture procedures.

U.S. FDA — Device Enforcement · United States · 2013-02-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0835-2013
Date of alert
2013-02-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Greiner Bio-One North America, Inc.
Product category
device
Product type
Devices
Reported risk: The VACUETTE Safety Blood Collection Set + Luer Adapter may display leaking (small droplets) during use due to a crack on the luer connector piece.
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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