Recall Z-0955-2023— Covidien, LLC

Name: FDA recall Z-0955-2023
Creator: U.S. Food and Drug Administration
Published: 2022-11-23

Class II · Ongoing

Class II FDA medical device recall by Covidien, LLC, initiated 2022-11-23. FDA's recall record names no specific 510(k) clearance for this event. Product: COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1. Reason: The product is labeled with the incorrect expiration date..

Recalling firm: Covidien, LLC
Classification: Class II
Status: Ongoing
Initiated: 2022-11-23
Firm location: Minneapolis, MN, United States

Product description

COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1

Reason for recall

The product is labeled with the incorrect expiration date.

Data sourced from openFDA. This site is unofficial and independent of the FDA.