Recall Z-2808-2015— Bard Access Systems

Name: FDA recall Z-2808-2015
Creator: U.S. Food and Drug Administration
Published: 2015-07-20

Class II · Terminated

Class II FDA medical device recall by Bard Access Systems, initiated 2015-07-20, terminated 2017-02-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Marketing brochures for the PowerPICC and PowerPICC SOLO catheters. Reason: Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure..

Recalling firm: Bard Access Systems
Classification: Class II
Status: Terminated
Initiated: 2015-07-20
Terminated: 2017-02-10
Firm location: Salt Lake City, UT, United States

Product description

Marketing brochures for the PowerPICC and PowerPICC SOLO catheters

Reason for recall

Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure.

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