B. Braun recalls CONT STIM Basic Kit with specific batch numbers due to potential catheter connector leakage. This could lead to disconnection during use, risking medication delivery errors. Affected units include batch numbers 61606946, 61613536, and 61619213.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
B. Braun is recalling certain CONT STIM Basic Kits with specific batch numbers because the catheter connectors may not stay closed, leading to possible leakage or disconnection. This could cause medication delivery issues during procedures.
The catheter connectors in these kits may not stay securely closed during use. This can lead to leakage or disconnection of the catheters from the connectors, potentially causing medication delivery errors during procedures.
Physicians using the CONT STIM Basic Kit for anesthetic and fluid administration are most at risk. The recall affects specific batch numbers of the kit.
Check the batch number on the kit label. Affected units include batch numbers 61606946, 61613536, and 61619213.
Look for the batch number on the kit label to confirm if it is affected.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of the catheters.
Batch numbers 61606946, 61613536, and 61619213.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3327-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3327-2018 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.
