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Lower risk Medical device recall · FDA · Published April 8, 2024

Medline Centurion CVC Kits Risk Patient Health Due to Leaks and Breakage

Medline recalls Centurion procedure kits with specific pack numbers and lot dates due to leaks and breakage risks that could harm patients during medical procedures.

🇺🇸 FDA recall #Z-2516-2024Medical deviceMedline ›
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Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer

Medline is recalling two types of Centurion procedure kits that contain plastic syringes prone to leaks and breakage. This could pose a risk to patient health during medical procedures. Read more at govinfonow.com/recall/55464-medline-centurion-cvc-kits-risk-patient-health-due-to-leaks.

Source Summary by GovInfoNow · govinfonow.com/recall/55464-medline-centurion-cvc-kits-risk-patient-health-due-to-leaks · Updated August 18, 2026 · FDA enforcement record: FDA #Z-2516-2024

Cite this page

“Medline Centurion CVC Kits Risk Patient Health Due to Leaks and Breakage.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/55464-medline-centurion-cvc-kits-risk-patient-health-due-to-leaks. Based on FDA recall #Z-2516-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2516-2024%22&limit=1).

The FDA announced on April 8, 2024, that Medline Industries LP is recalling Centurion procedure kits due to plastic syringes with potential leaks or breakage. Owners should stop using the affected kits immediately.

How to tell if you have it

  • Brand: Medline
  • Product: Centurion procedure kits labeled as CVC INSERT BUNDLE 16CM, Pack Number ECVC3260
  • Product: Centurion procedure kits labeled as CVC DOUBLE LUMEN 16CM, Pack Number ECVC8105
  • Lot Number: 2021031650 (Pack ECVC3260)
  • Lot Number: 2023012490 (Pack ECVC8105)

The hazard

The recalled medical convenience kits contain plastic syringes affected by an FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and other quality issues have been identified that may pose a risk to patient health.

Context

GovInfoNow's records show Medline Industries LP has issued 119 other recalls since October 22, 2021. Recent brand recalls include light failures in newborn resuscitation kits on July 25, 2025, and incorrect labeling in Foley Tray Kits on July 23, 2025. Other recent recalls of similar products include Medline IV Sets May Leak Chemicals and Break (December 31, 2025) and Medline Medical Kits Recall: Risk of Syringe Disconnection During Use (February 27, 2026).

How to tell if you have this one

Check for pack numbers ECVC3260 or ECVC8105 on the kits. Lot numbers 2021031650 and 2023012490 are also associated with these recalled items.

  • Brand
    Medline
  • Category
    Medical device
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Worldwide distribution.
Recall numberProduct, codes & lotsQuantity
Z-2515-2024Centurion procedure kits labeled as NEURO ANGIO PACK, Pack Number DYNDA1431A; Lot Number 2019072590—
Z-2516-2024Centurion procedure kits labeled as: 1) CVC INSERT BUNDLE 16CM, Pack Number ECVC3260; 2) CVC DOUBLE LUMEN 16CM, Pack Number ECVC8105; 1) ECVC3260, Lot Number 2021031650; 2) ECVC8105, Lot Number 2023012490—
Based on the official FDA remedy

What to do — step by step

  1. Check Kit Details

    Verify the pack number and lot number on the kit to confirm if it is recalled.

How this recall unfolded

Recall timeline

FDA published this recall 4 months after the firm started it.

1. Firm started the recall: Apr 8, 202412. FDA classified it Class II: Aug 7, 202423. Published in FDA’s Enforcement Report: Aug 14, 202432024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #Z-2516-2024 (April 8, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2516-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA