Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1142-2020 — 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.

U.S. FDA — Device Enforcement · United States · 2020-01-29 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1142-2020
Date of alert
2020-01-29
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Abbott Vascular
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08717648196003
Reported risk: Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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