B Braun recalls ADDitIV IV sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and UDI-DIs.
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
B Braun is recalling ADDitIV IV administration sets that can cause medication to flow backward into the main IV line or become blocked. This could lead to incorrect dosing or infections if the sets are used improperly.
The sets can allow medication from a secondary IV container to flow back into the primary IV line. This may cause the IV line to become blocked, making it impossible to properly prime the set and leading to incorrect medication delivery.
Healthcare professionals using IV pumps with B Braun's Infusomat series are most at risk. Patients receiving IV treatments with these sets may face incorrect medication dosing.
Check for catalog numbers V1443, V1447, V1448, or V1484 on the product label. Also look for the corresponding UDI-DI codes listed in the recall notice.
Look for catalog numbers V1443, V1447, V1448, or V1484 on the IV set label.
Reach out to B Braun Medical Inc for specific guidance on handling affected units.
The sets can cause medication to flow backward into the primary IV line and become blocked, leading to incorrect dosing or infections.
ADDitIV sets with catalog numbers V1443, V1447, V1448, or V1484 used with B Braun's Infusomat pumps.
No, but you should check your labels and contact B Braun if you have an affected unit.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0603-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0603-2026 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.
