B. Braun recalls Outlook IV Set 15Drop W/3 CareSite used with infusion pumps. Potential backflow of medication between IV containers could cause patient injury. All units distributed after August 1, 2:15 PM, 2023 are affected.
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.
B. Braun is recalling Outlook IV Set 15Drop W/3 CareSite used with infusion pumps. The backcheck valve might malfunction, causing medication to flow backward between IV containers and potentially causing patient injury.
The backcheck valve in the IV set might not work properly, allowing medication from a secondary IV container to flow back into the primary container. This could cause medication to not be properly administered, leading to patient injury.
Healthcare professionals using the Outlook IV Set 15Drop W/3 CareSite with infusion pumps are most at risk. Patients receiving IV medication through this system could be affected if the valve malfunctions.
Check for the model number 354213 or UDI-DI 04046964182211 on the product. The affected units were distributed after August 1, 2023.
Look for the model number 354213 or UDI-DI 04046964182211 on the product.
The backcheck valve might malfunction, causing medication to flow backward between IV containers and potentially causing patient injury.
All units distributed after August 1, 2023 are affected.
The recall record does not specify a remedy.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2377-2024 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2377-2024 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.
