Devices

Device Recall Plastic Kit

  • Model / Serial
    Lot number and expiration date  86626, 9/3/2017 87202, 9/16/2017 87481, 9/9/2017 87924, 9/17/2017 88217, 10/31/2017 88819, 10/27/2017 89271, 10/11/2017 89539, 12/7/2017 95831, 1/9/2018 96460, 4/12/2018 98055, 6/30/2018 98962, 6/22/2018 99088, 9/15/2018
  • 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
    Plastic Kit, part number CMP1084(C
  • 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

One device with a similar name

Learn more about the data here

Device Recall Plastic Kit
  • Model / Serial
    Lot number and expiration date  101684, 8/21/2018 84576, 5/19/2017 87746, 10/15/2017 88702, 11/13/2017 89228, 10/1/2017 95000, 1/16/2018 96841, 1/8/2018 97168, 6/11/2018 97250, 7/15/2018 99100, 6/9/2018
  • 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
    Plastic Pack, part number PSS2462 || Plastic Pack, part number PSS3319 || Plastic Pack, part number PSS3319(A
  • Manufacturer
    Windstone Medical Packaging, Inc.