Devices

Device Recall Basic Extended Pack

  • Modèle / numéro de série
    Lot number and expiration date  84855, 8/6/2018 88319, 9/5/2018 88950, 11/15/2018 95760, 1/26/2019 96235, 5/14/2019 98080, 6/19/2019
  • 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
    Basic Extended Pack, part number AMS4421(A || Basic Extended Pack, part number AMS4421(B
  • 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