Medline recalls namic convenience kits with excess material in female luer fittings that could cause blockages. Affected kits have specific model numbers and lot numbers listed in the recall notice.
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Medline is recalling namic convenience kits that have excess material near the fluid pathway in the female luer fittings. This could cause blockages during use, potentially leading to improper fluid flow in medical applications.
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway. This excess material could potentially cause blockages during use, which might lead to improper fluid flow in medical applications.
Healthcare professionals and medical facilities that use these namic convenience kits are most at risk. The recall affects specific model numbers and lot numbers listed in the notice.
Check for model numbers and lot numbers listed in the recall notice. Affected kits include specific references like REF60010468, REF60010511, and other model numbers with corresponding lot numbers.
Review the model numbers and lot numbers listed in the recall notice to determine if your kit is affected.
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway, which could cause blockages during use.
Check for model numbers and lot numbers listed in the recall notice, such as REF60010468, REF60010511, and other specific references with corresponding lot numbers.
Review the model numbers and lot numbers to determine if your kit is affected; no specific action is required beyond checking the details.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1431-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1431-2025 from Medline. 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.
