B. Braun recalls Safeline Y-Type Blood Sets (Catalog V2500) with potential leakage at blood filter-tubing joints. Affected units include specific lot numbers expiring through June 2024. Contact for remedy.
Potential for leakage at the joint between the blood filters and tubing
B. Braun is recalling Safeline Y-Type Blood Sets with catalog number V2500 due to a potential leakage risk at the joint between blood filters and tubing. This could lead to blood loss or contamination during medical procedures.
The blood filter and tubing joint may leak blood during use, potentially causing blood loss or contamination. This could lead to complications during medical procedures if the leak occurs.
Healthcare professionals and patients using the Safeline Y-Type Blood Set with catalog number V2500 are affected. Those using the product for blood transfusions or procedures are most at risk.
Check for the catalog number V2500 on the product. Affected units have specific lot numbers: 61674884, 61677634, 61678262, 61680625, and 61685110, expiring through June 2024.
Look for the catalog number V2500 and the specific lot numbers listed in the recall notice.
The recall indicates a potential leakage risk at the joint between blood filters and tubing, so it is not recommended for use until the remedy is applied.
The recall does not specify a remedy, so contact B. Braun Medical for further instructions.
Check for the catalog number V2500 and lot numbers: 61674884, 61677634, 61678262, 61680625, or 61685110, expiring through June 2024.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0941-2020 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-0941-2020 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.