B. Braun recalls Outlook Pump Sets with 3 CARESITE needle-free injection sites 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 Sets with 3 CARESITE needle-free injection sites because they can leak, leading to medication delays, under-dosing, or infections. This affects patients using these pumps for infusion therapy.
The pump sets can leak within the cassette portion, which may cause medication delays, under-delivery of doses, or incomplete dosing. This leakage can also lead to bloodstream infections if medication is not administered properly.
Patients using the Outlook Pump Sets for infusion therapy are most at risk. The recall applies to specific model numbers and production lots.
Check for the model name 'Outlook Pump Sets w/3 CARESITE Needle-Free Injection Sites' and production lots listed in the description: 0061755638 through 00VL754131.
Identify the lot code on your pump set, which should match the listed production lots (0061755638 to 00VL754131).
The recalled model is 'Outlook Pump Sets w/3 CARESITE Needle-Free Injection Sites' for use with the Outlook Safety Infusion System or Horizon NXT Pump.
Leakage can cause delays in medication administration, under-delivery of doses, incomplete dosing, or bloodstream infections.
Check the lot code on your pump set against the listed production lots: 0061755638 through 00VL754131.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2545-2021 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2545-2021 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.