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Bard Access Systems recalls Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
Recalled September 30, 2015 · FDA recall Z-2808-2015 · Bard Access Systems
Hazard
Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure. · FDA Class II
Units
1811
Sold at
Distributed to domestic and foreign conference attendees.
Description
Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure.
Product
Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
Manufacturer(s)
Bard Access Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →