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

Ultrasound Video Bronchoscope The EB-1970UK, Ultrasound Video Bronchoscope, is intended to provide optical visualization of, ultrasonic visualization of, and therapeutic access to, the Pulmonary Track including but not restricted to organs, tissues, and subsystem: Nasal Passage, Pharynx, Larynx, T — recall Z-0757-2017

U.S. FDA — Device Enforcement · United States · 2016-05-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0757-2017
Date of alert
2016-05-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Pentax of America Inc
Product category
device
Product type
Devices
Reported risk: The EB-1970UK Ultrasound Video Bronchoscope shipped between the clearance date of April 2014 and September 2015 contained the Operation and Reprocessing IFUs that were in use prior to the 2014 clearance, and therefore did not include the cleared Operation and Reprocessing IFUs.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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