Reported Mar 13, 2013 · Terminated

Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedures. Model numbers:…

Medtronic Inc. Cardiac Rhythm Disease Management

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: Medtronic Inc. Cardiac Rhythm Disease Management · 8200 Coral Sea St NE · Saint Paul, MN · 55112-4391

Is this the product you have?

  • Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedures
  • Model numbers
    • 67312
    • 67314
    • CB67314
    • 67316
    • 67318
    • CB67318
    • 67320
    • 69312
    • 69314
    • 69316
    • 69318
    • 69320
    • 69322
    • 69324
    • 69328
    • 69331
Lot codes and dates
  • Model Catalog# Lot

    285 of 285 codes

    • 67312
    • 6731210NO
    • 2012090293
    • 67312
    • 6731210NO
    • 2012090294
    • 67312
    • 6731210NO
    • 2012090337
    • 67312
    • 6731210NO
    • 2012100039
    • 67312
    • 6731210NO
    • 2012100086
    • 67312
    • 6731210NO
    • 2012100087
    • 67312
    • 6731210NO
    • 2012100161
    • 67312
    • 6731210NO
    • 2012110326
    • 67312
    • 6731210NO
    • 2012110767
    • 67312
    • 6731210NO
    • 2012110899
    • 67312
    • 6731210NO
    • 2012111721
    • 67314
    • 6731410NO
    • 2012090416
    • 67314
    • 6731410NO
    • 2012090435
    • 67314
    • 6731410NO
    • 2012090571
    • 67314
    • 6731410NO
    • 2012090572
    • 67314
    • 6731410NO
    • 2012100040
    • 67314
    • 6731410NO
    • 2012100041
    • 67314
    • 6731410NO
    • 2012100107
    • 67314
    • 6731410NO
    • 2012101346
    • 67314
    • 6731410NO
    • 2012110007
Amount recalled
13,691 (6711 USA; 6980 OUS)

Where it was sold

  • Nationwide

Why it was recalled

Potential for uncharacteristically rough metal edges to occur along the inner diameter of the metal tip side ports of the cannula.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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 21, 2013 · Data as of Sep 19, 6:54 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.