Devices

Device Recall Lumbar Laminectomy Pack

  • Modèle / numéro de série
    Lot number and expiration date  83672, 5/11/2018 84748, 6/3/2018 86722, 8/19/2018 88051, 1/7/2018 89026, 11/21/2018 89027, 12/12/2018 89882, 12/10/2018 94933, 1/29/2019
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    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.
  • Description du dispositif
    Lumbar Laminectomy Pack, part number AMS2501 || Lumbar Laminectomy Pack, part number AMS2501(A || Lumbar Laminectomy Pack, part number AMS2501(B
  • Manufacturer
    Windstone Medical Packaging, Inc.
  • 1 Event

Fabricant

Windstone Medical Packaging, Inc.
  • Adresse du fabricant
    Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
  • Société-mère du fabricant (2017)
    Windstone Medical Packaging Inc.
  • Source
    USFDA