B Braun Medical recalls ADDitIV IV sets used with Infusomat pumps due to risk of medication backflow and inability to prime. Affected units have specific catalog numbers and model labels.
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 ADDitIV IV administration sets that can cause medication to flow backward into primary IV containers and fail to prime properly. This could lead to incorrect dosing or infections if used in medical settings.
The sets may allow medication from secondary IV containers to flow back into the main container, causing incorrect dosing. They also may not prime correctly, leading to blockages or incomplete medication delivery.
Healthcare professionals using these IV sets with Infusomat pumps are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors.
Check for the label 'PB602VSL NON-VENT SET 103-IN-DR' with catalog number 352062. These sets were sold with Infusomat Space pumps from the manufacturer.
Look for the label 'PB602VSL NON-VENT SET 103-IN-DR' with catalog number 352062 on the set.
Reach out to B Braun Medical for guidance on whether the set is affected and next steps.
The recalled sets have the label 'PB602VSL NON-VENT SET 103-IN-DR' with catalog number 352062.
Check for the label 'PB602VSL NON-VENT SET 103-IN-DR' with catalog number 352062 on the set.
The recall does not specify an immediate stop; healthcare professionals should check the label and contact B Braun Medical for guidance.
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-0605-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0605-2026 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.
