Medline recalls Centurion Infusion Catheters with mislabeled antimicrobial heparin coating that may be distributed in medical kits. Affected lots include specific serial numbers and dates.
Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.
Medline is recalling certain Centurion Infusion Catheters that were mislabeled as having antimicrobial heparin coating. This mislabeling could lead to improper use in medical settings, potentially causing infections or other complications.
The catheters were mislabeled as having antimicrobial heparin coating when they actually do not. This could lead to improper use in medical settings, increasing the risk of infections or other complications.
Healthcare professionals and medical facilities that use these catheters may be affected. Patients receiving treatments with the recalled catheters are at risk of infection due to improper coating.
Check for the lot numbers: 2024103190, 2024050990, 2024021290, 2024012990, 2024111990. The catheters are part of the Centurion line with model numbers MIC17F7 and antimicrobial heparin coating.
Look for lot numbers 2024103190, 2024050990, 2024021290, 2024012990, or 2024111990 on the catheter packaging.
The recalled catheters are Centurion Infusion Catheters, 7F, 17cm (DO), Reorder MIC17F7 with antimicrobial heparin coating.
Check for lot numbers: 2024103190, 2024050990, 2024021290, 2024012990, or 2024111990.
The recall does not specify a remedy, so contact Medline directly 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-1048-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1048-2025 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.
