B Braun recalls specific IV administration sets used with pumps. These sets may allow medication to flow backward into the main container, causing potential contamination. Affected units have catalog numbers 490315, 490331, or 490376.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun is recalling certain IV administration sets that could allow medication to flow backward into the main container, risking contamination. This hazard occurs when the sets are used with gravity or pump systems, potentially causing serious infection or incorrect dosing.
The IV sets may allow medication from a secondary container to flow back into the primary container. This can happen if the sets are not properly primed, leading to potential contamination or incorrect dosing of medication.
Healthcare professionals using these IV sets with B Braun pumps are most at risk. Patients receiving IV treatments with the recalled sets could face contamination or incorrect medication dosing.
Check for catalog numbers 490315, 490331, or 490376 on the IV sets. These sets were sold with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Look for catalog numbers 490315, 490331, or 490376 on the IV administration set.
Reach out to B Braun Medical Inc for guidance on safe alternatives or replacements.
The sets may allow medication to flow backward into the primary container, causing potential contamination or incorrect dosing.
The recall applies to IV sets used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check for catalog numbers 490315, 490331, or 490376 on the IV set.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0664-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0664-2026 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.
