Reported May 20, 2020 · Terminated

PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D

Becton Dickinson & Company

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: Becton Dickinson & Company · 1 Becton Dr · Franklin Lakes, NJ · 07417-1815

Is this the product you have?

  • PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10
  • cm length Catalog NumberST018101D
Lot codes and dates
  • Lot NumberREDW0476 20 Exp
  • Date20OCT30
  • UDI(01)00801741139390
Amount recalled
655 kits

Where it was sold

Why it was recalled

Iincorrectly packaged without the required lidocaine as labeled

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 Oct 21, 2020 · Data as of Sep 19, 5:30 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.