April 30, 2020 / 5:22 PM / 25 days ago

BRIEF-FDA Says Vascular Solutions Recalls Langston Dual Lumen Catheter Due To Risk Of Separation During Use

April 30 (Reuters) - U.S. FDA:

* FDA SAYS VASCULAR SOLUTIONS RECALLS LANGSTON DUAL LUMEN CATHETER DUE TO RISK OF SEPARATION DURING USE

* FDA SAYS VASCULAR SOLUTIONS RECALLED 4,304 LANGSTON DUAL LUMEN CATHETER DEVICES IN THE U.S.

* FDA SAYS THERE HAVE BEEN 8 COMPLAINTS AND NO REPORTS OF INJURY OR DEATH RELATED TO VASCULAR SOLUTIONS LANGSTON DUAL LUMEN CATHETER

* FDA SAYS IT IDENTIFIED VASCULAR SOLUTIONS LANGSTON DUAL LUMEN CATHETER RECALL AS A CLASS I RECALL Source text: (bit.ly/2yUReys) Further company coverage:

0 : 0
  • narrow-browser-and-phone
  • medium-browser-and-portrait-tablet
  • landscape-tablet
  • medium-wide-browser
  • wide-browser-and-larger
  • medium-browser-and-landscape-tablet
  • medium-wide-browser-and-larger
  • above-phone
  • portrait-tablet-and-above
  • above-portrait-tablet
  • landscape-tablet-and-above
  • landscape-tablet-and-medium-wide-browser
  • portrait-tablet-and-below
  • landscape-tablet-and-below