B Braun Medical recalls IV administration sets used with gravity and pump systems 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 Medical is recalling certain IV administration sets used with gravity and pump 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 not addressed.
The IV sets can allow medication from a secondary container to flow back into the primary container, which may cause incorrect dosing or contamination. They also may not prime correctly, leading to blockages that could interrupt treatment.
Healthcare professionals using these IV sets with gravity or pump systems, particularly those in hospitals or clinics. Patients receiving IV treatments are at risk if the sets are not properly checked.
Check for catalog number 457506 on the set. These sets were sold with BBMI's Infusomat Space, Outlook, and Vista Basic pumps. The unit of dose UDI-DI is 04046964716119.
Look for catalog number 457506 or unit of dose UDI-DI 04046964716119 on the IV set.
Reach out to B Braun Medical for guidance on whether the set is affected and next steps.
The affected sets were used with BBMI's Infusomat Space, Outlook, and Vista Basic pumps.
Check for catalog number 457506 or unit of dose UDI-DI 04046964716119 on the set.
Contact B Braun Medical for guidance on whether the set is affected and next steps.
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-0646-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0646-2026 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.
