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 used with certain Infusomat pumps because they can cause medication to flow backward into the main IV line and fail to prime properly. This could lead to incorrect dosing or infections if not fixed.
The sets can allow medication from secondary IV containers to flow back into the primary IV line, potentially causing incorrect dosing. They may also fail to prime properly, leading to blockages or incomplete medication delivery.
Healthcare professionals using these IV sets with Infus: 1. V1782F UNIV IV SET W/0.2 MICRON FILTER (Catalog Number: 352447) with specific UDI-DIs. Patients receiving IV treatments through these sets are at risk of medication errors.
Check for the V1782F UNIV IV SET W/0.2 MICRON FILTER with catalog number 352447. Look for the primary UDI-DI 04046964181665 and unit of use UDI-DI 04046964181658 on the packaging or label.
Look for the catalog number 352447 and UDI-DIs 04046964181665 and 04046964181658 on the set packaging or label.
The V1782F UNIV IV SET W/0.2 MICRON FILTER with catalog number 352447.
The sets can cause medication to flow backward into the primary IV line and fail to prime properly, leading to incorrect dosing or blockages.
Check the product labels for the catalog number 352447 and UDI-DIs. If you have the affected set, contact B Braun for guidance.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0604-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0604-2026 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.
