B Braun Medical recalls Vista IV sets used with Infusomat 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 Vista IV sets used with certain Infus: 1. The sets could allow medication to flow backward from secondary to primary IV containers. 2. This could cause the IV to become blocked, making it impossible to prime the set properly.
The Vista sets can allow medication to flow backward from secondary (piggyback) IV containers into primary IV containers. This can cause the IV line to become blocked, making it impossible to prime the set properly. If not addressed, this could lead to treatment interruptions or medication errors.
Healthcare professionals using the Vista sets with B Braun's Infusomat pumps are most at risk. Patients receiving IV treatments with these sets may experience medication backflow or blockages.
Check for the catalog number US9923F on the Vista set. The set is labeled for use with B Braun's Infusomat Space, Outlook Pump, and Vista Basic Pump. Units have an expiration date of 36 months from manufacturing.
Look for the catalog number US9923F on the Vista set to confirm it is affected.
The sets can allow medication to flow backward from secondary to primary IV containers and cause the IV to become blocked, making it impossible to prime.
The recall does not specify a remedy, so check the set label for the catalog number US9923F to confirm if it is affected.
The sets have an expiration date of 36 months from manufacturing, as indicated on the label.
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-0715-2026 — B Braun Medical B Braun Medical Hello, I own a B Braun Medical that is covered by recall Z-0715-2026 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.
