B. Braun Medical recalls 60 drops/ml infusion pumps with potential leakage causing medication delays or bloodstream infections. Affected units sold with Outlook Safety Infusion System or Horizon NXT Pump.
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 Medical is recalling certain 60 drops/ml infusion pumps that may leak, causing medication delays or incomplete dosing. This could lead to bloodstream infections if not properly managed.
The pumps may leak within the cassette portion, causing medication delays or incomplete dosing. This could lead to bloodstream infections if the leakage affects the medication delivery.
Patients using the recalled pumps for infusion therapy are most at risk. Healthcare providers administering these pumps to patients may also be affected.
Check for the product name '60 drops/ml, Priming volume: 25 ml, Length: 120 in.' sold with Outlook Safety Infusion System or Horizon NXT Pump. Affected units have lot codes 0061758630 or 0061763934.
Verify the product name and lot code to confirm if your pump is affected.
Reach out to B. Braun Medical for specific guidance on next steps.
The recalled pump is 60 drops/ml with priming volume: 25 ml, length: 120 in., used with Outlook Safety Infusion System or Horizon NXT Pump.
Check for the product name and lot codes 0061758630 or 0061763934 on the pump packaging.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send B. Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2547-2021 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall Z-2547-2021 from B. Braun Medical. 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.
