Devices

Device Recall Major Kit

  • Modèle / numéro de série
    Lot number and expiration date  84334, 6/8/2018 86584, 8/7/2018 89801, 1/24/2019 96122, 3/6/2019 97375, 6/2/2019 98632, 6/3/2019
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.
  • Description du dispositif
    Major Kit, part number PHC1307(A
  • Manufacturer
    Windstone Medical Packaging, Inc.
  • 1 Event

Fabricant

Windstone Medical Packaging, Inc.
  • Adresse du fabricant
    Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
  • Société-mère du fabricant (2017)
    Windstone Medical Packaging Inc.
  • Source
    USFDA