B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential backflow of medication and inability to prime. Affected units have specific catalog numbers and expiration dates.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun Medical is recalling IV administration sets used with gravity and pump systems because they can cause medication to flow backward into the main container and fail to prime properly. This could lead to incorrect dosing or infections if the set is not used correctly.
The IV set can allow medication from a secondary container to flow back into the primary container during use. This can cause incorrect dosing or contamination if the set is not properly primed, potentially leading to infections or treatment errors.
Healthcare professionals using IV administration sets with B Braun Medical's Infusomat, Outlook, or Vista pumps are most at risk. Patients receiving IV treatments with these sets may also be affected.
Check for the catalog number 354208 on the set. These units were sold with B Braun Medical's Infusomat, Outlook, or Vista pumps and have an expiration date of 24 months from the date of manufacture.
Look for the catalog number 354:208 on the IV administration set.
The sets can cause medication to flow backward from secondary containers into primary containers and may not prime properly, leading to incorrect dosing or contamination.
The recall affects IV sets used with B Braun Medical's Infusomat Space, Outlook, and Vista Basic pumps.
Check for the catalog number 354208 on the set, which was sold with specific pumps and has an expiration date of 24 months from manufacture.
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-0684-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0684-2026 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.
