B Braun recalls Outlook 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 is recalling Outlook IV sets used with 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 Outlook set can allow medication from secondary IV containers to flow back into the primary IV line. It also fails to prime correctly, which may cause blockages or incorrect 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 catalog number 490564 on the set. These units were sold with Infusomat pumps like the Space Large Volume Pump, Outlook Pump, or Vista Basic Pump. Expiration dates are listed on the packaging.
Look for catalog number 490564 on the set or packaging. Verify expiration date and pump compatibility.
The Outlook set can cause medication to flow backward into the primary IV line and fail to prime correctly, which may lead to incorrect dosing or infections.
The recall record does not specify a remedy, so contact B Braun Medical Inc directly for guidance.
Check for catalog number 490564 on the set or packaging. These units were sold with Infusomat pumps like the Space Large Volume Pump, Outlook Pump, or Vista Basic Pump.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0708-2026 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-0708-2026 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.
