B Braun recalls anesthesia IV sets used with certain pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and pump models.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun is recalling anesthesia IV sets used with gravity and pump administration systems. This recall is due to a risk of medication backflow from secondary IV containers into primary containers and the inability to properly prime the set, which could lead to incorrect dosing.
The IV set may allow medication from a secondary container to flow back into the primary container. This can cause incorrect dosing of medication. The set may also not prime properly, leading to blockages or incomplete medication delivery.
Healthcare professionals using the recalled IV sets with B Braun pumps are most at risk. Patients receiving anesthesia through these sets could be affected if the sets are not properly primed.
Check for catalog number 490476 on the IV set. These sets were sold with B Braun's Infusomat Space, Outlook, and Vista Basic pumps. The product was labeled as 'IV ADMIN SET, 2-HIGH FLOW STPCKS, 124 IN'.
Look for catalog number 490476 on the IV set label.
Reach out to B Braun Medical Inc for further assistance if you have the recalled product.
The recall affects IV sets used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
Check for catalog number 490476 on the IV set label. These sets were sold with specific B Braun pumps.
The recall record does not specify a remedy, so contact B Braun Medical Inc directly for assistance.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0613-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0613-2026 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.
