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Teleflex, Inc. recalls White Bronchial Double Lumen Tube Set (Right) Sterile
Recalled August 26, 2015 · FDA recall Z-2414-2015 · Teleflex
Hazard
Customer complaints reporting that the cobb connector detached from the main connector prior to use. · FDA Class II
Sold at
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Description
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Product
White Bronchial Double Lumen Tube Set (Right) Sterile
Manufacturer(s)
Teleflex, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →