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 number 490:612.
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 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 contamination of the medication.
The IV sets can allow medication from a secondary container to flow back into the primary container, potentially causing incorrect dosing or contamination. They may also fail to prime properly, leading to blockages or incomplete medication delivery.
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 may also be affected.
Check for the catalog number 490612 on the set. These sets were sold with B Braun's Infusomat, Outlook, or Vista pumps and have an expiration date of 36 months from manufacture.
Look for the catalog number 490612 on the IV administration set.
Reach out to B Braun Medical Inc for guidance on next steps if you have the recalled set.
The catalog number is 490612.
The affected pumps are Infusomat Space, Outlook, and Vista Basic.
Check for the catalog number 490612 on the set, which was sold with B Braun's Infusomat, Outlook, or Vista pumps.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0677-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0677-2026 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.
