B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential backflow of medication and inability to prime. Affected units include 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 certain 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 infections if not addressed.
The IV sets can allow medication from secondary containers to flow back into the primary container, potentially causing incorrect dosing. They may also fail to prime correctly, leading to blockages or incomplete medication delivery.
Healthcare professionals using these IV sets with gravity or pump systems, particularly those administering medications via piggyback infusions. Patients receiving IV treatments with these sets are at risk of medication errors.
Check for the catalog number 490354 on the IV set. These sets were sold with specific expiration dates and are used with B Braun's Infusomat Space, Outlook, or Vista Basic pumps.
Look for the catalog number 4903:54 on the IV set label.
The sets can cause medication to flow backward from secondary containers into primary containers and may fail to prime correctly, leading to incorrect dosing or blockages.
These sets are used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check for the catalog number 490354 on the IV set label, which was sold with specific expiration dates.
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-0693-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0693-2026 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.
