B Braun recalls specific IV administration sets used with gravity and pump systems due to potential backflow of medication and inability to prime. Affected units have catalog numbers 354210 or 490389.
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 IV line and fail to prime properly. This could lead to incorrect dosing or infections if not fixed.
The IV sets can allow medication from a secondary (piggyback) container to flow back into the primary IV line. This can cause incorrect dosing or infections. Additionally, the sets may not prime properly, leading to blockages that disrupt treatment.
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 catalog numbers 354210 or 490389 on the IV sets. These sets were sold with B Braun's Infusomat, Outlook, or Vista pumps between the dates listed in the product descriptions.
Look for catalog numbers 354210 or 490389 on the IV set packaging or label.
Reach out to B Braun Medical Inc for guidance on next steps if you have the recalled sets.
IV sets with catalog numbers 354210 or 490389 used with B Braun's Infusomat, Outlook, or Vista pumps.
The sets can cause medication to flow backward into the primary IV line and may not prime properly, leading to incorrect dosing or infections.
No, but you should check the catalog number and contact B Braun if you have the affected 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-0654-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0654-2026 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.
