B. Braun Medical recalls Infusomat UNIV 15 Drop Pump Sets (model 362431) sold after August 2, 2:15, 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 Medical is recalling Infusomat UNIV 15 Drop Pump Sets sold after August 2, 2023. The pump set may cause medication to flow backward into the main IV line, leading to patient injuries like adverse drug reactions or medication loss.
The backcheck valve in the pump set might malfunction, allowing medication from a secondary IV container to flow back into the primary IV container. This can cause medication to not be properly primed, leading to patient injuries such as adverse drug reactions or loss of medication.
Healthcare professionals using the Infusomat UNIV 15 Drop Pump Set for IV medication administration are most at risk. Patients receiving IV treatments with this pump set could experience medication backflow injuries.
Check for the model number 362431 on the pump set. The product was distributed after August 2, 2023, and includes the UDI-DI 04046964294013.
Look for the model number 362431 on the pump set to confirm it is recalled.
Reach out to B. Braun Medical for further guidance on handling the recalled product.
The model number is 362431.
The product was distributed after August 2, 2023.
The UDI-DI number is 04046964294013.
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-2383-2024 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall Z-2383-2024 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.
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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.
