Device Recall Abdominoplasty Pack

  • Modèle / numéro de série
    Lot numbers and Expiration dates:  80483, 1/19/2017 86796, 2/26/2018 88290, 2/7/2017 89931, 1/15/2018 98043, 9/7/2018 98446, 4/2/2019
  • 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
    Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
  • 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