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

6" (15 cm) Appx 0.85 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 2 Check Valve, 3 Clamps, Rotating Luer; — recall Z-1724-2022

U.S. FDA — Device Enforcement · United States · 2022-08-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1724-2022
Date of alert
2022-08-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
ICU Medical, Inc.
Product category
device
Product type
Devices
Reported risk: Due to a manufacturing defect which results in a visible gap between the connector's top and bottom housing.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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