B Braun recalls specific IV administration sets that may cause medication backflow and inability to prime, potentially leading to incorrect dosing. Affected sets include models with catalog numbers 354209, 490392, and 490428.
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. These sets could allow medication to flow backward into the main IV line and fail to prime properly, risking incorrect dosing for patients.
The recalled IV sets may allow medication from a secondary (piggyback) container to flow back into the primary IV line. This can cause incorrect dosing if the set fails to prime properly, potentially leading to unsafe medication levels.
Healthcare professionals using these IV sets for patient care are most at risk. Patients receiving IV treatments with the recalled sets could face incorrect medication dosing.
Check for the following catalog numbers: 354209, 490392, or 490428. These sets are used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Identify the catalog number on the set's label to confirm if it's affected.
Reach out to B Braun Medical Inc for guidance on next steps if the set is recalled.
The hazard is potential backflow of medication from secondary IV containers into primary containers and the inability to prime the set, which could lead to incorrect dosing.
The affected models have catalog numbers 354209, 490392, and 490428, used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
No, but you should check the catalog number and contact B Braun Medical Inc for specific instructions if you have the recalled sets.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0648-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0648-2026 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.
