Device Recall LifeShield I.V. Pump Set

  • Modèle / numéro de série
    Lot numbers: 521815H, 571015H, and 571615H.
  • 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
    Lifeshield, latex-free, Primary I.V. Pump Set with Distal Microbore Patient Line and Gravity Flow Prevention Valve, convertible pin, 110 inch with high-pressure filter, orange polyethylene-lined/light resistant tubing and OPTION-LOK for use with OMNI-FLOW infusion system, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 12163-01.
  • 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