B. Braun Medical recalls Infusomat SPACE PUMP IV sets (model 362432) sold after August 2, 2: Potential backflow of medication causing patient injuries. Affected units have UDI-DI 04046964182679.
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 SPACE PUMP IV sets that could allow medication to flow backward into the main IV line, risking patient injuries. This recall affects units distributed after August 2, 2023, with specific model and UDI-DI numbers.
The backcheck valve in the IV set might malfunction, causing medication from secondary IV containers to flow backward into the primary IV line. This can lead to patient injuries like adverse drug reactions or medication loss.
Healthcare professionals using the Infusomat SPACE PUMP IV set for intravenous medication administration are most at risk. Patients receiving IV treatments with this specific set could experience medication backflow injuries.
Check for the model number 362432 on the product. The recall includes units distributed after August 2, 2023, with UDI-DI number 04046964182679.
Verify the model number (362432) and UDI-DI (04046964182679) on the Infusomat SPACE PUMP IV set.
The model number is 362432.
Units distributed after August 2, 2023.
The UDI-DI number is 04046964182679.
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-2384-2024 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall Z-2384-2024 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.
