B. Braun recalls 30 ML 2PORT BURET: Manufacturing issue may cause leakage, increasing infection risk and delaying therapy. Affected units include specific lot numbers.
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.
B. Braun is recalling 30 ML 2PORT BURETTE ASSEMBLIES due to a manufacturing issue that can cause leakage. This leakage may delay therapy, increase bloodstream infection risk, and expose patients and healthcare workers to hazardous medication. There is also a potential for life-threatening situations requiring additional medical intervention.
The device may leak due to a manufacturing defect. This leakage can delay medical therapy, increase the risk of bloodstream infections, and expose both patients and healthcare workers to hazardous medication. In severe cases, it may lead to life-threatening situations requiring additional medical intervention.
Healthcare facilities using the 30 ML 2PORT BURETTE ASSEMBLY (Article No. 7A3950) in contrast management systems are affected. Patients and healthcare workers using the device are at risk of infection or life-threatening complications.
Check for the product name '30 ML 2PORT BURETTE ASSEMBLY' with Article No. 7A3950. Affected units were sold with lot number 0061766049.
Immediately stop using the 30 ML 2PORT BURETTE ASSEMBLY if it is part of the recalled lot.
No, the product has a manufacturing issue that can cause leakage, increasing infection risk and potentially leading to life-threatening situations.
Immediately stop using it and contact B. Braun for further instructions.
Lot number 0061766049 is affected.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0131-2024 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-0131-2024 from B. Braun. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
