B. Braun recalls UNIV 15 Drop Pump Set (model 363433) sold after August 3, 2: Risk of medication backflow causing patient injuries. Stop using immediately.
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.
B. Braun is recalling its Infusomat UNIV 15 Drop Pump Set (model 363433) sold after August 3, 2023. The backcheck valve may malfunction, causing medication to flow backward into the primary IV line, which could lead to patient injuries or medication loss.
The backcheck valve might fail, allowing medication from a secondary IV container to flow back into the primary IV line. This could cause patient injuries, medication loss, or improper treatment.
Patients using this specific IV pump set for medication delivery are affected. Healthcare providers administering IV treatments with this model are most at risk.
Check for the model number 363433 on the pump set. The product was sold after August 3, 2023, and has a UDI-DI code 04046964837920.
Discontinue use of the Infusomat UNIV 15 Drop Pump Set (model 363433) as it poses a risk of medication backflow.
The model number is 363433.
The product was sold after August 3, 2023.
The recall record does not mention a fix or remedy.
We’ve drafted a message you can send B. Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2393-2024 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall Z-2393-2024 from B. Braun Medical. 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.
