Device Recall General Plastics Pack

  • Model / Serial
    Lot number and expiration date  85096, 12/11/2017 85458, 12/20/2017 88364, 12/27/2017 89172, 9/3/2018 95260, 9/20/2018 95790, 9/9/2018 96288, 9/18/2018 96562, 9/20/2018 97526, 9/27/2018 97560, 9/13/2018 99232, 2/1/2019 99232, 2/1/2019
  • Product Classification
  • 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
    General Plastics Pack, part number 008617-1
  • Manufacturer
  • 1 Event

Manufacturer

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