B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow 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 in gravity and pump IV 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 contamination of the medication.
The IV sets can allow medication from secondary containers to flow back into the primary container, potentially causing contamination. They may also not prime correctly, leading to blockages or incorrect medication delivery.
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 490519 on the IV set. These sets were sold with B Braun Medical's Infusomat, Outlook, or Vista pumps and have an expiration date of 36 months from manufacture.
Look for the catalog number 490519 on the IV administration set.
Reach out to B Braun Medical for guidance on next steps if you have the recalled set.
The recalled IV set has catalog number 490519 and is used with B Braun Medical's Infusomat, Outlook, or Vista pumps.
Check for the catalog number 490519 on the set label. These sets were sold with specific B Braun Medical pumps and have an expiration date of 36 months from manufacture.
Contact B Braun Medical directly for guidance on next steps, as the recall remedy is not specified in the record.
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-0672-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0672-2026 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.
