Bard Access Systems recalls Marketing brochures for the PowerPICC and PowerPICC SOLO catheters

Recall date

July 20, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2808-2015

FDA classification

Class II

Brand / firm

Bard Access Systems

Sold / distributed

Distributed to domestic and foreign conference attendees.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Marketing brochures for the PowerPICC and PowerPICC SOLO catheters