Devices

Device Recall Hernia Pack

  • Model / Serial
    Lot number and expiration date  101167, 5/30/2019 87349, 6/20/2018 88830, 9/11/2018 89510, 11/29/2018 94616, 11/15/2018 94704, 11/24/2018 95209,11/25/2018 95934, 1/15/2019 97409, 3/6/2019 99486, 3/12/2019
  • 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
    Hernia Pack, part number AMS3859
  • 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