B. Braun recalls Y-Type Blood Pump Sets with potential leakage causing medication delays, under-delivery, or bloodstream infections. Affected units include specific lot codes and model numbers for the Outlook Safety Infusion System.
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 Y-Type Blood Pump Sets that may leak, causing medication delays, under-delivery, or infections. This affects users of the Outlook Safety Infusion System or Horizon NXT pumps.
The pump sets can leak within the cassette portion, leading to medication delays, incomplete dosing, or bloodstream infections. This happens when the pump set is used with the Outlook Safety Infusion System or Horizon NXT pumps.
Users of the Outlook Safety Infusion System or Horizon NXT pumps with the recalled Y-Type Blood Pump Sets are most at risk. This includes patients receiving parenteral fluids through these devices.
Check for the model name 'Y-Type Blood, Outlook Pump Set, Caresite-single-use' with lot code 0061772, and the serial number 04046955202799. The product was sold with the Outlook Safety Infusion System or Horizon NXT pumps.
Look for the lot code 0061772234 and serial number 04046955202799 on the pump set packaging.
The Y-Type Blood, Outlook Pump Set, Caresite-single-use for use with the Outlook Safety Infusion System or Horizon NXT pumps.
Leakage can cause medication delays, under-delivery of doses, incomplete dosing, or bloodstream infections.
Check for the lot code 0061772234 and serial number 04046955202799 on the pump set packaging.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2553-2021 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2553-2021 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.
