B. Braun recalls Infusomat UNIV 60 Drop Pump Set (model 363423) sold after August 4, 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 60 Drop Pump Sets made after August 4, 2023, because a faulty backcheck valve could cause medication to flow backward into the main IV line, risking patient injury. This affects patients receiving IV treatments with this specific pump set.
The backcheck valve may malfunction, allowing medication from secondary IV containers 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.
Patients using the Infusomat UNIV 60 Drop Pump Set for intravenous medication administration are most at risk. Healthcare facilities and home care users who have this model are affected.
Check for the model number 363423 on the pump set. The product was distributed after August 4, 2023, and includes two care sites for IV use.
Look for model number 363423 on the Infusomat UNIV 60 Drop Pump Set.
Reach out to B. Braun Medical Inc for assistance with the recall process.
The model number is 363423.
The pump set was distributed after August 4, 2023.
Check for the model number 363423 and ensure it was distributed after August 4, 2023.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2390-2024 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2390-2024 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.
