B Braun recalls specific IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have catalog numbers 477002 or 477017.
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 used with gravity or pump infusion systems because they might cause medication to flow backward into the main container and fail to prime properly. This could lead to incorrect dosing or treatment errors.
The IV sets may allow medication from a secondary container to flow back into the primary container during use. This can cause incorrect dosing or treatment errors if the sets cannot be properly primed to check for blockages.
Healthcare professionals using these IV sets with B Braun's Infusomat, Outlook, or Vista pumps are most at risk. Patients receiving IV treatments with these specific sets could be affected.
Check for catalog numbers 477002 or 477017 on the IV sets. These sets were sold with B Braun's Infusomat, Outlook, or Vista pumps between the dates listed in the product description.
Look for catalog numbers 477002 or 477017 on the IV administration set.
Reach out to B Braun Medical Inc for guidance on next steps if you have the affected sets.
The sets may allow medication to flow backward into the primary container and fail to prime properly, which could lead to incorrect dosing or treatment errors.
These sets were used with B Braun's Infusomat, Outlook, and Vista Basic pumps.
Check for catalog numbers 477002 or 477017 on the IV administration 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-0702-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0702-2026 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.
