B. Braun recalls Infusomat SPACE PUMP SET 15 DROP W/2 SAFEDAY models distributed after August 1, 2: Risk of medication backflow causing patient injuries. Contact for remedy.
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 SET 15 DROP W/2 SAFEDAY IV pumps made after August 1, 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 pump could fail, allowing medication from a secondary IV container to flow back into the primary IV container. This might cause medication to be administered incorrectly, leading to adverse drug reactions or loss of medication.
Healthcare professionals using the Infusomat SPACE PUMP SET 15 DROP W/2 SAFEDAY for IV medication administration are most at risk. Patients receiving IV treatments with this pump could be affected if the valve malfunctions.
Check for the model number 362420 on the pump. The product was distributed after August 1, 2023, with UDI-DI 04046955592715.
Look for the model number 362420 and distribution date after August 1, 2023.
The pump has a potential risk of medication backflow if the backcheck valve malfunctions, which could cause patient injuries.
The recall record does not specify a remedy, so contact B. Braun Medical for further instructions.
The recall applies to pumps distributed after August 1, 2023.
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-2382-2024 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall Z-2382-2024 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.
