Devices

Device Recall Pack

  • Model / Serial
    Lot number and expiration date  101356, 9/9/2019 83800, 3/13/2018 89442, 10/3/2018 94546, 11/21/2018 95128, 6/30/2019
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    2
  • Implanted device?
    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.
  • Product Description
    Robotic Pack, part number AMS4389
  • Manufacturer
    Windstone Medical Packaging, Inc.
  • 1 Event

Manufacturer

Windstone Medical Packaging, Inc.
  • Manufacturer Address
    Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
  • Manufacturer Parent Company (2017)
    Windstone Medical Packaging Inc.
  • Source
    USFDA