B Braun recalls SAFELINE IV sets used with Infusomat pumps due to potential medication backflow and inability to prime, which could cause errors in IV administration.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun is recalling SAFELINE IV sets used with Infusomat pumps because they can cause medication to flow backward into the main IV line and fail to prime properly. This could lead to incorrect medication delivery and patient harm.
The SAFELINE sets can allow medication from secondary IV containers to flow back into the primary IV line. They may also become blocked (occluded) when trying to prime, which can cause medication errors during IV administration.
Healthcare professionals using these IV sets with Infusomat pumps are most at risk, particularly those administering medications to patients via intravenous therapy.
Check for the following catalog numbers: 352604, NF1251, or NF1290. These sets are used with Infusomat pumps like Space, Outlook, or Vista Basic models.
Identify the catalog number on the product label to confirm if it's a recalled SAFELINE set.
Reach out to B Braun Medical Inc for assistance with the recall process.
The sets can allow medication to flow backward into the primary IV line and may become blocked when trying to prime, potentially causing medication errors.
The recalled sets are used with Infusomat Space, Outlook, and Vista Basic pumps.
Look for catalog numbers 352604, NF1251, or NF1290 on the product label.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0713-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0713-2026 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.