Devices

Device Recall LifeShield Secondary I.V. Set

  • Modèle / numéro de série
    Lot numbers: 530964W, 530974W, 530984W, 530994W, 531014W, 531024W, 531034W, 531044W, 531054W, 531064W, 531074W, 531084W, 531094W, 531104W, 531114W, 531754W, 540644W, 540654W, 540664W, 540674W, 540684W, 540694W, 540704W, 540714W, 540724W, 540734W, 540744W, 540754W, 540764W, 540774W, 540784W, 540794W, 550654W, 550664W, 550684W, 550694W, 550704W, 550714W, 550724W, 550734W, 550744W, 550754W, 550764W, 550774W, 550784W, 550794W, 550804W, 550824W, 551044W, 560134W, 560144W, 560154W, 560284W, 560294W, 560304W, 560314W, 560324W, 560334W, 560344W, 560354W, 560364W, 560374W, 560384W, 560394W, 560404W, 570414W, 570424W, 570434W, 570524W, 570534W, 570544W, 570554W, 570564W, 570574W, 570584W, 570594W, 570604W, 570614W, 570624W, 570634W, 570644W, 580044W, 580054W, 580064W, 580504W, 580514W, 580524W, 580534W, 580544W, 580554W, 580564W, 580574W, 580584W, 580594W, 580604W, 580624W, 581274W, 590094W, 590104W, 590114W, 590124W, 590134W, 590144W, 590154W, 590164W, 590174W, 590194W, 590204W, 590214W, 590224W, 590234W, 590244W, 591544W, 600284W, 600574W, 600584W, 600594W, 600604W, 600614W, 600624W, 600634W, 600644W, 600654W, 600674W, 600684W, 600694W, 600704W, 600714W, 610794W, 610804W, 610814W, 610824W, 610834W, 610844W, 610854W, 610864W, 610874W, 610884W, 610894W, 610904W, 610914W, 610924W, 620404W, 620414W, 620424W, 620434W, 620444W, 620454W, 620494W, and 620504W.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • 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
    Lifeshield, latex-free Secondary I.V. Set, convertible pin, 32 inch, piggyback with OPTION-LOK, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 11953-48.
  • Manufacturer
    Hospira Inc.
  • 1 Event

Fabricant

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

3 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

Device Recall LifeShield Secondary I.V. Set
  • Modèle / numéro de série
    Lot numbers: 541264W, 551074W, 560224W, 560934W, 561264W, 561304W, 561314W, 561324W, 570504W, 580914W, 581334W, 591304W, 600824W, 600834W, 611534W, 620564W, and 621064W.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • 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
    Lifeshield, latex-free, Secondary I.V. Set, convertible pin, 32 inch with OPTION-LOK, drop-in blunt cannula and Snap Lok, 15 drops/mL, a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; list 11397-58.
  • Manufacturer
    Hospira Inc.
Device Recall LifeShield Secondary I.V. Set
  • Modèle / numéro de série
    Lot numbers: 541284W, 541294W, 571154W, 610114W and 610124W.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • 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
    Lifeshield, latex-free, Secondary I.V. Set, convertible pin, 32 inch, piggyback with drop-in blunt cannula and OPTION-LOK, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 11954-48.
  • Manufacturer
    Hospira Inc.
Device Recall LifeShield Secondary I.V. Set
  • Modèle / numéro de série
    Lot numbers: 531264W, 531274W, 601594W and 621065H.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • 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
    Lifeshield, latex-free Secondary I.V. Set, convertible pin, 34 inch, piggyback with OPTION-LOK, non-DEHP, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 12667-28.
  • Manufacturer
    Hospira Inc.