Devices

Device Recall Open Procedure Pack

  • Modelo / Serial
    Lot number and expiration date  100206, 6/1/2018 100248, 7/9/2018 100438, 7/19/2018 100439, 8/29/2018 100853, 9/15/2018 86832, 10/10/2017 88268, 10/4/2017 89377 ,11/9/2017 89378, 12/9/2017 94967, 12/31/2017 95888, 1/5/2018 96199, 2/11/2018 97018, 1/9/2018 97019, 2/17/2018 97146, 4/28/2018 97301, 3/22/2018 97478, 6/13/2018 98189, 5/20/2018
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    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.
  • Descripción del producto
    Open Procedure Pack, part number AMS4596 || Open Procedure Pack, part number AMS4596(A || Open Procedure Pack, part number AMS4596(B
  • Manufacturer
    Windstone Medical Packaging, Inc.
  • 1 Event

Fabricante

Windstone Medical Packaging, Inc.
  • Dirección del fabricante
    Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
  • Empresa matriz del fabricante (2017)
    Windstone Medical Packaging Inc.
  • Source
    USFDA

Dispositivo con un nombre similar

Más información acerca de la data acá

Device Recall Open Procedure Pack II
  • Modelo / 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
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    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.
  • Descripción del producto
    Open Procedure Pack II, part number RMS1740(A
  • Manufacturer
    Windstone Medical Packaging, Inc.