B. Braun recalls 15 drops/ml infusion pump sets with potential for under-dosing, incomplete medication delivery, and bloodstream infections due to leakage in cassette portions.
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 specific 15 drops/ml infusion pump sets that may leak, causing medication under-delivery, incomplete dosing, or bloodstream infections. This affects patients using these pumps for parenteral fluid administration.
The pump sets can leak within the cassette portion, leading to delays in medication delivery, incomplete dosing, and potential bloodstream infections. This occurs because the leakage affects the precise measurement of fluids during infusion therapy.
Patients using the recalled pump sets for infusion therapy are most at risk. Healthcare providers administering these pumps to patients may also be affected.
Check for the product name '15 drops/ml, Priming Volume: 27ml, Length: 129 in.' and lot codes listed in the recall notice. The pump sets are designed for use with the Outlook Safety Infusion System or Horizon NXT Pump.
Identify the product by checking the label for the 15 drops/ml, Priming Volume: 27ml, Length: 129 in. specifications and lot codes listed in the recall notice.
The recall involves 15 drops/ml, Priming Volume: 27ml, Length: 129 in. single-use pump sets designed for use with the Outlook Safety Infusion System or Horizon NXT Pump.
The pump sets may leak, causing delays in medication delivery, incomplete dosing, or bloodstream infections.
Check the label for the product specifications and lot codes listed in the recall notice.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2544-2021 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2544-2021 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.
