B Braun Medical recalls anesthesia IV sets used with certain pumps due to potential backflow of medication between IV containers, risking contamination and inability to prime.
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 anesthesia IV sets used with specific IV pumps because they can cause medication to flow backward between IV containers and fail to prime properly. This could lead to contamination or incorrect dosing if the set is used without proper checks.
The IV set may allow medication from a secondary (piggyback) container to flow back into the primary container. This can cause contamination or prevent the set from being properly primed, leading to incorrect dosing or treatment errors.
Healthcare professionals using the recalled IV sets with B Braun pumps are most at risk. Patients receiving IV treatments with these sets could face medication errors or contamination.
Check for the label 'IV ADMIN SET, 15D, 144 IN.' with catalog number 490472. These sets were sold with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Look for the label 'IV ADMIN SET, 15D, 144 IN.' with catalog number 490472 on the set.
The IV set can allow medication to flow backward between containers and fail to prime properly, risking contamination or incorrect dosing.
These sets were used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check for the label 'IV ADMIN SET, 15D, 144 IN.' with catalog number 490472 on the set.
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-0610-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0610-2026 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.
