Abbott Vascular: Medical Device Recall in 2020 - (Recall #: Z-1142-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

NC TRAVELER Coronary Dilatation Catheter, REF 1013157-15, Rx Only,NC Traveler RX 4.0 X 15MM The NC Traveler RX Coronary Dilatation Catheter is not cleared for commercial distribution in the United States.

Product Classification:

Class I

Date Initiated: January 29, 2020

Date Posted: February 26, 2020

Recall Number: Z-1142-2020

Event ID: 84826

Reason for Recall:

Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.

Status: Terminated

Product Quantity: Total 791 Traveler (0 US and 791 OUS)

Code Information:

Device Identifier/GTIN: 08717648196003 Part Number: 1013157-15 Lot Numbers:91102G1

Distribution Pattern:

Worldwide Distribution: US (Nation-wide) and OUS (countries of): Algeria Jordan Argentina Korea Armenia Kuwait Aruba Lebanon Australia Malaysia Austria, Mauritius Bahrain Mexico Bangladesh Morocco Belgium Netherlands Brazil New Zealand Brunei Norway Bulgaria Oman Canada Pakistan Chile Panama China Peru Colombia Poland Costa Rica Portugal Croatia R¿union Cyprus Romania Czech Republic Russian Federation Denmark Saudi Arabia Dominican Republic Singapore Egypt Slovakia Estonia Slovenia Finland South Africa France Spain Germany Sri Lanka Greece State of Palestine Hong Kong Sweden Hungary Switzerland Iceland Taiwan, Province of China India Thailand Indonesia Tunisia Iran Turkey Iraq Ukraine Ireland United Arab Emirates Israel United Kingdom Italy Uruguay Japan Viet Nam

Voluntary or Mandated:

Voluntary: Firm initiated