B. Braun recalls Infusomat UNIV. 15 Drop Pump Sets (model 363230) sold after August 1, 2023, due to potential backflow of medication causing patient injuries.
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 Infusomat UNIV. 15 Drop Pump Sets sold after August 1, 2023, because a faulty backcheck valve might cause medication to flow backward into the primary IV container, risking patient injury. This could lead to adverse drug reactions or medication loss.
The backcheck valve in the pump could malfunction, allowing medication from secondary IV containers to flow back into the primary container. This might cause medication to be lost or lead to adverse drug reactions in patients.
Healthcare professionals using the Infusomat pump for IV medication administration are most at risk, particularly those with the specific model sold after August 1, 2023.
Check for the model number 363230 on the pump set. The product was sold after August 1, 2023, with UDI-DI 04046964294495.
Look for the model number 363230 on the Infusomat UNIV. 15 Drop Pump Set.
Reach out to B. Braun Medical Inc for guidance on next steps if the pump is affected.
The affected model is Infusomat UNIV. 15 Drop Pump Set with model number 363230.
The product was sold after August 1, 2023.
The recall record does not specify 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-2403-2024 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2403-2024 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.
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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.
