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

Tracheopart Set (Right), Sterile — recall Z-2413-2015

U.S. FDA — Device Enforcement · United States · 2014-11-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2413-2015
Date of alert
2014-11-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Teleflex, Inc.
Product category
device
Product type
Devices
Reported risk: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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