B Braun recalls specific IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include model 470005 with certain catalog numbers.
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 in gravity and pump IV systems because they can cause medication to flow backward into the main container and fail to prime properly. This could lead to incorrect dosing or infections if the set is used without proper checks.
The IV sets can allow medication from secondary containers to flow back into the primary container, which may cause incorrect dosing. They also may not prime correctly, leading to blockages that could cause medication to not flow as intended.
Healthcare professionals using these IV sets with B Braun's Infusomat, Outlook, or Vista pumps are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors.
Check for the catalog number 470005 on the set. These sets were sold with B Braun's Infusomat, Outlook, or Vista pumps and labeled as 'IV SET 15DR 3 CARESITE, 124 IN.'
Look for the catalog number 470005 on the IV set label.
Reach out to B Braun Medical Inc for guidance on next steps if you have the recalled set.
The recalled set has catalog number 470005, labeled as 'IV SET 15DR 3 CARESITE, 124 IN.'
The recall does not require immediate stop use; however, you should check if you have the recalled set and contact B Braun for guidance.
The recalled sets are used with B Braun's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0658-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0658-2026 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.
