Device Recall Breast Recon Pack

  • Modèle / numéro de série
    Lot number and expiration date  100592, 9/7/2019 96541, 6/16/2019 97532, 5/7/2019 97836, 6/4/2019 98247, 6/15/2019 98788, 6/29/2019
  • Classification du dispositif
  • 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
    Breast Recon Pack, part number AMS5698 || Breast Recon Pack, part number AMS5698(A
  • Manufacturer
  • 1 Event

Fabricant

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