B. Braun recalls ophthalmic administration sets with potential leakage causing infection, delayed therapy, and serious health risks. Affected units include specific model numbers and lots.
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.
B. Braun is recalling ophthalmic administration sets that may leak due to a manufacturing issue. This leakage can delay treatment, increase infection risk, and potentially cause serious health problems.
The administration sets may leak medication due to a manufacturing defect. This leakage can delay necessary eye treatments, increase the risk of bloodstream infections, and expose patients and healthcare workers to hazardous medication. In severe cases, it may require additional medical intervention.
Healthcare workers and patients using the recalled ophthalmic administration sets for eye procedures are most at risk. The specific model numbers and production lots listed in the recall affect those who have purchased the product.
Check for the model number 7A3817 and lot numbers 0061747706, 0061752064, 0061755195, or 0061790409 on the product packaging or label.
Look for the model number 7A3817 and lot numbers 0061747706, 0061752064, 0061755195, or 0061790409 on the product packaging or label.
The administration sets may leak due to a manufacturing issue, which can delay therapy, increase infection risk, and potentially cause serious health problems.
Check the product for the model number 7A3817 and lot numbers 0061747706, 0061752064, 0061755195, or 0061790409. If you have the recalled product, contact B. Braun for further instructions.
Yes, the leakage could lead to life-threatening situations requiring additional medical intervention.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-0130-2024 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-0130-2024 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.
