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Recall Observatory FDA recall evidence

Device product

Marketing brochures for the PowerPICC and PowerPICC SOLO catheters

Z-2808-2015

July 20, 2015

Class II

Product summary

Firm
Bard Access Systems
Event
Event 71757
Status
Terminated
Classification
Class II
Quantity
1811
Official record key
device-enforcement:Z-2808-2015

Official wording

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.

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

Distribution pattern: Distributed to domestic and foreign conference attendees.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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