Bard Access Systems: Medical Device Recall in 2015 - (Recall #: Z-2808-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Marketing brochures for the PowerPICC and PowerPICC SOLO catheters

Product Classification:

Class II

Date Initiated: July 20, 2015

Date Posted: September 30, 2015

Recall Number: Z-2808-2015

Event ID: 71757

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.

Status: Terminated

Product Quantity: 1811

Code Information:

The brochures were purchased from the vendor on 04/14/2015, Code S120667R0

Distribution Pattern:

Distributed to domestic and foreign conference attendees.

Voluntary or Mandated:

Voluntary: Firm initiated