ClearanceBrief
Recall Z-1141-2020 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous

Abbott Vascular

NC TRAVELER Coronary Dilatation Catheter, REF 1013157-12, Rx Only,NC Traveler RX 4.0 X 12MM The NC Traveler RX Coronary Dilatation Catheter is not cleared for commercial distribution in the United States.

DateFeb 14, 2020 (initiated Jan 29, 2020)
StatusTerminated
ReasonCoronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
Root causeProcess change control
ActionOn 01/29/2020, the firm field personnel and Affiliates directly contacted the first customers beyond the firm's control via phone, email, or personal visit to facilitate rapid notification. The "URGENT MEDICAL DEVICE RECALL" Notification informed customers that specific lots of its Coronary Dilatation Catheters with diameters of 4.0 mm, 4.5 mm, and 5.0 mm may exhibit difficulty or inability to deflate the balloon due to weaker material proximal to the balloon bond resulting from excess heat exposure during manufacturing, and the potential risks with the use of the affected products include ai
QuantityTotal 791 Traveler (0 US and 791 OUS)
DistributionWorldwide Distribution: US (Nation-wide) and OUS (countries of): Algeria Jordan Argentina Korea Armenia Kuwait Aruba Lebanon Australia Malaysia Austria, Mauritius Bahrain
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K103153VOYAGER NC CORONARY DILATATION CATHETER AND NC TREK RX CORONARY DILATATION CATHETER
Abbott Vascular-Cardiac Therapies, Dec 30, 2010
K110134NC TREK RX CORONARY DILATATION CATHETER
Abbott Vascular-Cardiac Therapies, Feb 11, 2011