Device Recall Custom Venous Kit

  • Model / Serial
    Lot number and expiration date  84766, 1/8/2018 85230, 1/12/2018 85938, 1/7/2018 88327, 1/6/2018 88591, 1/9/2018 96129, 1/11/2018 96256, 1/1/2018 96660, 1/2/2018 98425, 1/24/2018
  • 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
    Custom Venous Kit, part number TVS4024(C
  • Manufacturer
  • 1 Event

Manufacturer

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