B. Braun recalls Outlook Pump Primary Administration Sets with micro tubing for epidural use due to potential leakage causing medication delays or bloodstream infections. Affected units sold with 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 Outlook Pump sets used for epidural medication delivery because they can leak, leading to medication delays, under-dosing, or infections. This is serious for patients receiving critical treatments.
The pump sets can leak within the cassette portion, which may cause medication delays, under-delivery of doses, or incomplete dosing. This leakage risk can lead to bloodstream infections if medication isn't administered properly.
Patients using the recalled Outlook Pump sets for epidural medication administration are most at risk. Healthcare providers who use these sets for parenteral fluid infusions may also be affected.
Check for the product name 'Outlook Pump Primary Administration Set w/ micro Tubing for Epidural Administration' sold with specific lot code 0061770205 or serial number DI: 04046964189388.
Immediately stop using the recalled Outlook Pump sets for epidural medication administration as they can leak, causing medication delays or infections.
The recalled product is the Outlook Pump Primary Administration Set with micro tubing for epidural administration, sold with lot code 0061770205 or serial number DI: 04046964189388.
Patients using the recalled pump sets may experience medication delays, under-dosing, or bloodstream infections due to leakage in the cassette portion of the pump.
The recall record does not mention a remedy or replacement option; the remedy field is null.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2559-2021 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2559-2021 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.
