B Braun Medical recalls RATE FLOW IV sets used with certain pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
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 RATE F: 15-drop IV sets used with gravity or pump administration systems. These sets can cause medication to flow backward into the main IV line or become blocked, which may lead to incorrect dosing or infections.
The RATE FLOW sets can allow medication from a secondary IV container to flow back into the primary IV line. This can cause incorrect dosing or infections. The sets may also become blocked (occluded), preventing proper medication flow.
Healthcare professionals using these IV sets with B Braun's Infusomat pumps are most at risk. Patients receiving IV treatments with the recalled sets could face medication errors.
Check for the catalog number 375258 on the set. These sets were sold with B Braun's Infusomat Space, Outlook, and Vista Basic pumps. The expiration date is the earliest expiration of components or 36 months from manufacture.
Look for catalog number 375258 on the RATE FLOW set. These sets were used with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
The RATE FLOW sets can cause medication to flow backward into the primary IV line or become blocked, leading to incorrect dosing or infections.
Check for catalog number 375258 on the set. These sets were sold with B Braun's Infusomat Space, Outlook, and Vista Basic pumps.
The recall does not specify a remedy, so contact B Braun Medical for guidance on safe use or replacement.
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-0710-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0710-2026 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.
