B Braun Medical recalls blood administration sets used with certain IV pumps due to potential medication backflow and inability to prime. Affected units have 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 blood administration sets used with gravity IV systems and specific pumps. The sets could allow medication to flow backward into the main container and fail to prime properly, which may cause medication errors.
The sets might let medication from secondary IV containers flow back into the primary container. They also may not prime correctly, leading to blockages that could cause medication errors.
Healthcare professionals using these sets with Infusomat, Outlook, or Vista Basic pumps are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors.
Check for catalog number 490530 on the set. The sets were sold with Infusomat, Outlook, or Vista Basic pumps from the manufacturer.
Look for catalog number 490530 on the blood administration set.
The recall affects blood administration sets used with Infusomat, Outlook, and Vista Basic pumps.
Check for catalog number 490530 on the set label.
The recall record does not specify a remedy or fix.
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-0618-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0618-2026 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.
