Reported Sep 30, 2015 · Terminated

Marketing brochures for the PowerPICC and PowerPICC SOLO catheters

Bard Access Systems

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Bard Access Systems · 605 N 5600 W · Salt Lake City, UT · 84116-3738

Is this the product you have?

  • Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
Lot codes and dates
  • The brochures were purchased from the vendor on 04/14/2015, Code S120667R0
Amount recalled
1811

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 10, 2017 · Data as of Sep 19, 4:45 PM UTC

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