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Home > Recalled Products > Medical Devices > Undetermined Hazard > NC Trek, NC Traveler, and NC Tenku NC Trek RX Coronary Dilatation Catheter, NC Traveler Coronary Dilatation Catheter, And NC Tenku RX PTCA Balloon Catheter

Recall: NC Trek, NC Traveler, and NC Tenku NC Trek RX Coronary Dilatation Catheter, NC Traveler Coronary Dilatation Catheter, And NC Tenku RX PTCA Balloon Catheter

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On 2017-05-15, the FDA announced that Abbott is conducting a recall on NC Trek RX Coronary Dilatation Catheter, NC Traveler Coronary Dilatation Catheter, And NC Tenku RX PTCA Balloon Catheter due to a possible undetermined hazard. The recalled products were sold under the brand name(s) NC Trek, NC Traveler and and NC Tenku during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 2 medical devices recalls due to potential undetermined hazard, including system controller and dc adapters, ventricular assist device and more. Additionally, there have been 3 drug and medical device recalls due to other health hazards as well as 130 food recalls.

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Company Contact Information:

Name: Abbott

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Detailed Recall Information



Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.

Product Description: NC Trek RX Coronary Dilatation Catheter, NC Traveler Coronary Dilatation Catheter, and NC Tenku RX PTCA Balloon Catheter

Brand Name(s): NC Trek, NC Traveler, and NC Tenku

Reason for Recall: Potential problems with inflating or deflating the catheter balloon

Official Recall Date: 2017-05-12

Note: Although this recall announcement is dated 05/12/2017, it was not published by the FDA until 05/15/2017.



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Additional information provided by the FDA.gov:

Abbott has initiated a voluntary recall of specific lots of three catheters: NC Trek RX Coronary Dilatation Catheter, NC Traveler Coronary Dilatation Catheter, and NC Tenku RX PTCA Balloon Catheter. Read More.


More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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