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

107" (272 cm) Ext Set w/2 Check Valves, MicroClave T-Connector, Clamp, Rotating Luer, Non-DEHP Tubing, Item No. B33041 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile. — recall Z-1589-2015

U.S. FDA — Device Enforcement · United States · 2015-04-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1589-2015
Date of alert
2015-04-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
ICU Medical, Inc.
Product category
device
Product type
Devices
Reported risk: ICU Medical is recalling MicroClave T-Connectors because they have potential connection separation issues that could lead to leakage.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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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.