B. Braun recalls 50-unit cartons of Extension Set (EXT SET W/CARESITE, 6IN.) due to high failure risk causing leaks, detachment, infections, and potential life-threatening issues.
The extension set has a high probability of failure which could lead to possible leakage or detachment at the device's bonded joint during use. The issue may result in delay of therapy, increased risk of bloodstream infections (BSI), and may expose both patients and healthcare workers to hazardous medications. Depending on the nature of the leak and type of infusion, there is also the potential for life-threatening situations to occur including air embolization or hypovolemia.
B. Braun is recalling extension sets that could leak or detach during use, risking infections and serious health problems. This affects IV equipment used in medical settings.
The extension set has a high probability of failing at its bonded joint, which can cause leaks or detachment. This may delay treatment, increase infection risk, and lead to life-threatening conditions like air embolization or severe blood loss.
Healthcare workers and patients using IV therapy with the recalled extension sets are most at risk due to potential leaks and detachment.
Look for the product name 'EXT SET W/CARESITE, 6IN.' with product code 470169. The extension sets come in cartons of 50 units.
Immediately stop using the recalled extension sets as they can cause leaks, detachment, and serious health risks.
The product code is 470169.
Each carton contains 50 units.
The recalled extension sets could cause leaks or detachment, leading to delayed therapy, increased risk of bloodstream infections, and potential life-threatening situations like air embolization or hypovolemia.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0091-2023 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-0091-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
