B. Braun recalls Outlook Pump Add-On Sets (Ref: V740: 0061765082) due to potential leakage causing medication delays, under-delivery, or bloodstream infections.
Leakage of the pump set within the cassette portion of the pump sets, potential for delays in administration of medications, under-delivery or incomplete dosing and bloodstream infections.
B. Braun is recalling Outlook Pump Add-On Sets that can leak, leading to medication delays, under-dosing, or infections. This affects patients using these pumps for infusion therapy.
The pump set can leak within the cassette, causing medication delays, under-delivery, or incomplete dosing. This increases the risk of bloodstream infections if medication isn't administered correctly.
Patients using Outlook Pump Add-On Sets with Outlook Safety Infusion System or Horizon NXT Pump for medication infusions are affected. Those with compromised immune systems or complex medical conditions face higher risk.
Check for the product name 'Outlook Pump Add-On Set' with reference number V7400 and lot code 0061765082. The product was sold with Outlook Safety Infusion System or Horizon NXT Pump.
Verify the reference number V7400 and lot code 0061765082 on the pump set packaging.
Reach out to B. Braun Medical for guidance on next steps if you have the recalled product.
Yes, the recall addresses potential leakage causing medication delays, under-delivery, or bloodstream infections.
Look for the reference number V7400 and lot code 0061765082 on the Outlook Pump Add-On Set packaging.
Check the product details and contact B. Braun Medical for guidance on next steps.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2558-2021 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2558-2021 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.
