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 have specific catalog numbers.
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 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 complications if the set is used without proper checks.
The IV sets can allow medication from secondary containers to flow back into the primary IV line, potentially causing incorrect dosing. They may also fail to prime correctly, leading to blockages or incomplete medication delivery.
Healthcare professionals and patients using IV therapy with gravity or pump systems may be affected. Those using the recalled sets with specific catalog numbers are most at risk.
Check for the catalog number 490357 on the IV set. These sets were sold with gravity IV systems and specific pump models like Infusomat Space, Outlook, and Vista Basic.
Look for the catalog number 490:357 on the IV administration set.
The recalled IV set has catalog number 490357 and is used with gravity IV systems and specific pump models like Infusomat Space, Outlook, and Vista Basic.
Check for the catalog number 490357 on the IV administration set. These sets were sold with gravity IV systems and specific pump models.
The recall record does not specify a remedy, so contact B Braun Medical for guidance.
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-0641-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0641-2026 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.
