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 490193 and 490326.
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 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 treatment errors.
The IV sets can allow medication from secondary containers to flow back into the primary container. This may cause incorrect dosing or treatment errors if the sets cannot be properly primed.
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.
Check for catalog numbers 490193 or 490326 on the product label. These sets were sold with B Braun's Infusomat Space, Outlook, or Vista Basic pumps.
Look for catalog numbers 490193 or 490326 on the IV set label.
Reach out to B Braun Medical Inc for guidance on next steps.
The sets can cause medication to flow backward into the primary container and fail to prime properly, leading to potential dosing errors.
Check for catalog numbers 490193 or 490326 on the product label, which were used with B Braun's Infusomat Space, Outlook, or Vista Basic pumps.
Contact B Braun Medical Inc for guidance on next steps, as the recall does not specify a return or replacement process.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0695-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0695-2026 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.
