Devices

Open Procedure Pack II

  • Model / Serial
    Lot Numbers/ Expiration Dates:  59942 4/3/2015 59692 4/19/2015 59858 11/25/2015 65398 11/30/2015 66543 7/4/2016 67496 9/14/2016 70943 1/31/2017 70944 8/11/2017 79014 9/17/2017 79771 1/10/2018
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.
  • Product Description
    Open Procedure Pack II, Kit number RMS1740(A || convenience custom kits used for general surgery in hospital operating room
  • 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 Open Procedure Pack II
  • Model / Serial
    Lot number and expiration date  84814, 2/6/2018 86168, 8/30/2018 88510, 12/1/2018 89151, 1/21/2019 95032, 1/13/2019 96555, 6/1/2019 98134, 6/6/2019 99502, 9/17/2019
  • 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
    Open Procedure Pack II, part number RMS1740(A
  • Manufacturer
    Windstone Medical Packaging, Inc.