Z-0131-2024 Class II Ongoing

Recalled by B. Braun Medical, Inc. — Allentown, PA

Recall Details

Product Type
Devices
Report Date
November 15, 2023
Initiation Date
September 26, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
350 units

Product Description

30 ML 2PORT BURETTE ASSEMBLY, Article No. 7A3950, used in a contrast management system.

Reason for Recall

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.

Distribution Pattern

Worldwide distribution - US Nationwide and the countries of Canada and Singapore.

Code Information

UDI-DI: N/A Lots 0061766049