B. Braun recalls Outlook Pump 15 Drop IV sets with 2 CARESITE Y-Sites due to leakage risk, potential medication delays, under-delivery, and bloodstream 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 certain IV sets that can leak, causing medication delays, under-dosing, or infections. This affects patients receiving IV treatments with these specific sets.
The IV set can leak within the cassette portion, leading to medication delays, under-delivery of doses, or incomplete dosing. This increases the risk of bloodstream infections for patients receiving IV treatments.
Patients using the recalled IV sets for infusion therapy are most at risk. Healthcare providers administering these sets may also be affected.
Check for the product name: Outlook Pump 15 Drop 0.2 Micron Filtered IV Set with 2 CARESITE Y-Sites. Affected units have lot codes 0061752471, 0061756801, 0061757861, 0061766196, or 0061777798.
Look for lot codes 0061752471, 0061756801, 0061757861, 0061766196, or 0061777798 on the packaging.
The IV set can leak within the cassette portion, causing medication delays, under-delivery of doses, or incomplete dosing, which may lead to bloodstream infections.
Check for the product name: Outlook Pump 15 Drop 0.2 Micron Filtered IV Set with 2 CARESITE Y-Sites. Affected units have lot codes 0061752471, 0061756801, 0061757861, 0061766196, or 0061777798.
No immediate stop is required, but you should check the lot code and contact B. Braun if you have the recalled product.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2546-2021 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2546-2021 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.
