B. Braun recalls Infusomat SPACE PUMP IV Set 15D (model 480254) sold after August 2, 2023. Potential backflow of medication could cause patient injuries. Affected users should contact B. Braun for details.
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 SPACE PUMP IV Set 15D models sold after August 2, 2023. The backcheck valve might malfunction, causing medication to flow backward into the primary IV line and potentially causing patient injuries.
The backcheck valve in the IV set might fail, allowing medication from secondary IV containers to flow back into the primary IV line. This could cause medication to be administered incorrectly, leading to patient injuries or product malfunction.
Healthcare professionals using the Infusomat SPACE PUMP IV Set 15D with electric infusion pumps for IV medication administration are most at risk. Patients receiving IV treatments through this system could be affected.
Check for the model number 480254 on the IV set. The product was distributed after August 2, 2023. It is used with electric infusion pumps for IV medication delivery.
Reach out to B. Braun Medical for specific instructions on how to handle the recalled IV set.
The recall indicates a potential risk of medication backflow, so it is not safe to use without contacting B. Braun for guidance.
The model number is 480254.
This product was distributed after August 2, 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-2394-2024 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2394-2024 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.
