B. Braun recalls 118-single-use V1500HP Outlook Pump Sets due to leakage risks that could cause medication delays, under-delivery, or infections. Affected units have specific lot codes.
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 118-single-use V1500HP Outlook Pump Sets that may leak, causing medication delays, under-delivery, or infections. This affects patients using these pumps for infusion therapy.
The pump sets can leak within the cassette portion, leading to medication delays, under-delivery, or incomplete dosing. This increases the risk of bloodstream infections if medication isn't delivered properly.
Patients using the V1500HP Outlook Pump Sets for infusion therapy are most at risk. The recall applies to specific lot codes produced between April 2023 and May 2023.
Check for lot codes: 0061756809, 0061763935, 0061768485, or 0061777803. These pump sets were sold with the Outlook Safety Infusion System or Horizon NXT Pump for infusion of parenteral fluids.
Look for lot codes 0061756809, 0061763935, 0061768485, or 0061777803 on the pump set packaging.
No, but you should check the lot code to see if your pump set is affected. If it is, contact B. Braun for instructions.
Leakage can cause medication delays, under-delivery, or incomplete dosing, increasing the risk of bloodstream infections.
Check the lot code on your pump set packaging. Affected units have specific lot codes: 0061756809, 0061763935, 0061768485, or 0061777803.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2551-2021 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2551-2021 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.
