B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include specific catalog numbers and pump models.
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 certain IV administration sets used with gravity and pump systems because they can cause medication to flow backward into the main IV container and fail to prime properly. This could lead to incorrect dosing or infections if the issue isn: t fixed.
The IV sets can allow medication from a secondary container to flow back into the primary container during use. This may also prevent the set from being properly primed, which is necessary to ensure the correct flow of medication.
Healthcare professionals using these IV sets with gravity or pump systems are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors or infections.
Check for the catalog number 490309 on the IV administration set. These sets were sold with specific pump models including Infusomat Space, Outlook, and Vista Basic pumps.
Look for the catalog number 490309 on the IV administration set.
The IV sets can cause medication to flow backward into the primary container and fail to prime properly, which may lead to incorrect dosing or infections.
The affected pumps include Infusomat Space, Outlook, and Vista Basic pumps.
Check for the catalog number 490309 on the IV administration set, which was sold with the mentioned pump models.
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-0661-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0661-2026 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.
