Medline recalls medical convenience kits with excess material in female luer fittings that could cause blockages. Affected kits have specific labels and lot numbers from 2019.
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Medline is recalling medical convenience kits that have excess material near the fluid pathway in female luer fittings. This could cause blockages during use, potentially leading to treatment delays or complications.
The excess material in the female luer fittings could block the fluid pathway, preventing proper flow of fluids. This might cause treatment delays or complications if the kit is used for critical medical procedures.
Healthcare workers using these kits in hospitals or clinics are most at risk. Patients receiving care with these kits may experience treatment delays or complications.
Check for kits labeled with MTS, COLOR, PML, KIT, -, FRENCH HOSPITAL PG. The lot number is 0000141266 and the reference number is 600605710.
Look for the label MTS,COLOR,PML,KIT,-,FRENCH HOSPITAL PG on the kit.
The female luer fittings have excess material near the fluid pathway that could cause blockages.
Check for the label MTS,COLOR,PML,KIT,-,FRENCH HOSPITAL PG and lot number 0000141266.
The recall does not specify a remedy, so contact Medline for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1430-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1430-2025 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.
