B Braun recalls SafeDAY IV sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun is recalling SafeDAY IV administration sets used with certain Infus: 1. IV ADM SET 15 DR W/2 SAFEDAY & STOPCOCK (catalog 352646) may cause medication to flow backward into the main IV line or fail to prime properly. This could lead to incorrect medication dosing if the set is not used correctly.
The SafeDAY sets can allow medication from secondary IV containers to flow back into the primary IV line. This may cause incorrect dosing if the set is not properly primed, potentially leading to unsafe medication administration.
Healthcare professionals using these IV sets with Infusomat pumps are most at risk. Patients receiving IV treatments with the recalled sets could experience medication errors.
Check for the catalog number 352646 on the set label. These sets were sold with Infusomat pumps like Space, Outlook, and Vista Basic models. The expiration date is 36 months from the start date.
Look for the catalog number 352646 on the set label to confirm if it is affected.
If you have the affected set, contact B Braun Medical Inc for further instructions.
The affected set is the IV ADM SET 15 DR W/2 SAFEDAY & STOPCOCK with catalog number 352646.
Check for the catalog number 352646 on the set label. These sets were sold with Infusomat pumps like Space, Outlook, and Vista Basic models.
Contact B Braun Medical Inc for further instructions. The remedy is not specified in the recall notice.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0712-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0712-2026 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.
