March 6, 2020 / 5:18 PM / a month ago

BRIEF-FDA Says Becton Dickinson Carefusion 303 Recalls Alaris System Infusion Pumps Due To Software, System Errors

March 6 (Reuters) - FDA-

* FDA- BECTON DICKINSON CAREFUSION 303 RECALLS ALARIS SYSTEM INFUSION PUMPS DUE TO SOFTWARE AND SYSTEM ERRORS

* FDA SAYS HAS IDENTIFIED ALARIS SYSTEM INFUSION PUMPS RECALL AS A CLASS I RECALL

* FDA- 774,000 ALARIS SYSTEM PUMPS RECALLED IN U.S.

* FDA SAYS BD/CAREFUSION 303 RECALLING ALARIS INFUSION PUMP SYSTEM & MODULES DUE TO MANY SYSTEM ERRORS WHICH HAVE CAUSED 55 REPORTED INJURIES, 1 DEATH

* FDA- ON FEB 4, BD/CAREFUSION 303 SENT LETTERS TO CUSTOMERS, STATING ALARIS PUMP MODELS ISSUES Source text: (bit.ly/2THqI2m) 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