B. Braun recalls UNIV.15DROP pump sets made after August 1, 2:15, 2023 due to potential medication backflow causing patient injuries. Affected units may need replacement.
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 certain Infusomat UNIV.15DROP pump sets made after August 1, 2023 because a backcheck valve might malfunction, causing medication to flow backward and potentially causing patient injuries. This could lead to adverse drug reactions or loss of medication.
The backcheck valve might fail, allowing medication from a secondary IV container to flow back into the primary container. This could cause medication to be lost or lead to adverse reactions in patients.
Healthcare professionals using the Infusomat pump set for intravenous medication administration are most at risk. Patients receiving IV treatments with these pumps could be affected if the valve malfunctions.
Check for the model number 362032 on the pump set. Units were distributed after August 1, 2023, and include the UDI-DI 04046964182556.
Look for model number 362032 on the pump set. Units distributed after August 1, 2023 are affected.
The backcheck valve might malfunction, causing medication to flow backward and potentially causing patient injuries like adverse drug reactions or loss of medication.
Check if your pump set has model number 362032 and was distributed after August 1, 2023. If so, contact B. Braun for further instructions.
Yes, the malfunction could cause medication backflow, leading to adverse drug reactions or loss of medication in patients.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2378-2024 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2378-2024 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.
