FDAJuly 20, 2015device
Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
Official recall recorded by the U.S. Food & Drug Administration.
The 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.
What to do
FDA enforcement status: Terminated
Brands named
bard access systemsbardbard access
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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