B Braun Medical recalls anesthesia IV sets that may cause medication backflow between IV containers, risking incorrect dosing. Affected sets include specific models sold with Infusomat pumps.
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 anesthesia IV sets used with gravity or pump administration systems. These sets could allow medication to flow backward from secondary to primary IV containers, potentially causing incorrect dosing if not properly primed.
The IV sets may allow medication to flow backward from a secondary (piggyback) IV container into the primary IV container. This can happen when the set is not properly primed, leading to potential incorrect dosing of medication.
Healthcare professionals using these IV sets during anesthesia procedures are most at risk. Patients receiving IV medication through these sets could experience incorrect dosing if the backflow occurs.
Check for the specific model labeled as 'IV ADMIN SET W/15 DROPS/ML, 134 IN.' with catalog number 490477. These sets were sold with Infusomat, Outlook, and Vista Basic pumps.
Look for the label indicating 'IV ADMIN SET W/15 DROPS/ML, 134 IN.' with catalog number 490477.
The sets may allow medication to flow backward from a secondary IV container into the primary container, causing incorrect dosing if not properly primed.
These sets were sold with Infusomat Space, Outlook, and Vista Basic pumps.
No, but you should check if you have the affected model and follow the instructions to ensure safe use.
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-0609-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0609-2026 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.
