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B. Braun Medical, Inc. recalls 30 ML 2PORT BURETTE ASSEMBLY, Article No. 7A3950, used in a contrast management system.
Recalled November 15, 2023 · FDA recall Z-0131-2024 · B. Braun Medical
Hazard
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention. · FDA Class II
Units
350 units
Sold at
Worldwide distribution - US Nationwide and the countries of Canada and Singapore.
Description
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.
Product
30 ML 2PORT BURETTE ASSEMBLY, Article No. 7A3950, used in a contrast management system.
Manufacturer(s)
B. Braun Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →