Reported Apr 20, 2016 · Terminated

USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.

US Endovascular

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Us Endovascular · 1150 Milwaukee St · Saint Louis, MO · 63122-7336

Is this the product you have?

  • USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.
Lot codes and dates
  • All references USE .014RX
  • Lot numbers

    314 of 314 codes

    • 1717082810164720
    • 1717082810164720
    • 1717082810164720
    • 1717082810164720
    • 1717082810164720
    • 1717082810164730
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166230
    • 1717101610166250
    • 1717101610166250
    • 1717082810164740
    • 1717101610166250
    • 1717101610166250
    • 1717082810164740
    • 1717101610166250
    • 1717101610166250
    • 1717082810164760
    • 1717101610166240
    • 1717082810164760
    • 1717082810164770
    • 1717082810164770
    • 1717101610166260
    • 1717101610169180
    • 1717101610169180
    • 1717101610169180
    • 1717101610166260
    • 1717101610169180
    • 1717101610166260
    • 1717082810164770
    • 1717101610166260
    • 1718041510177220
    • 1717082810164770
    • 1717101610169180
    • 1717082810164780
    • 1717101610166270
    • 1717082810164780
    • 1717101610166270
    • 1717101610166270
    • 1717101610169190
    • 1717082810164800
    • 1717101610169190
    • 1717101610169190
    • 1717101610169190
    • 1717101610166280
    • 1717082810164810
    • 1717082810164810
    • 1717101610166290
    • 1717082810164810
    • 1717082810164810
    • 1717101610166290
Amount recalled
843 catheters

Where it was sold

Why it was recalled

Product may kink during use rendering the product unusable.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 30, 2017 · Data as of Sep 19, 5:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.