Device Recall Hospira Midlength Secondary I.V. Set

  • Modèle / numéro de série
    Lot numbers: 530764W, 530774W, 540464W, 550484W, 550494W, 560924W, 561334W, 570494W, 570984W, 570994W, 580014W, 590834W, 591134W, 611004W, 611014W, 611364W, 611374W, and 620554W.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- U.S., Puerto Rico, Dominican Republic, Bahamas, Virgin Islands, Argentina, Australia, Bahrain, Belgium, Canada, China, Denmark, Ecuador, EI Salvador, Finland, France, Germany, Greece, Guatemala, Hong Kong, Ireland, Italy, Jordan, Kuwait, Lebanon, Libya, Mexico, Netherlands, New Zealand, Nicaragua, Norway, Oman, Panama, Peru, Philippines, Poland, Portugal, San Marino, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Kingdom, Uruguay, and United Arab Emirates.
  • Description du dispositif
    Latex-free. Midlength Secondary I.V. Set, convertible pin, 40 inch with extension hook for use with OMNI-FLOW Medication Management System and PLUM Series Infusions Systems, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 1139-48.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Hospira Inc., 375 N Field Dr, Lake Forest IL 60045-2513
  • Société-mère du fabricant (2017)
  • Source
    USFDA