Device Recall Dr. Wischmeier Pack

  • Modèle / numéro de série
    Lot numbers:  75870 78661 79154 81580 81800 83500 83594 83680 84118 84262 86073 86485 86887 87119 89180 95109 95422 95809 96760 97589 98512 99060 100410 101234
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution including CA, CO, FL, GA, IA, KY, MA, MN, MO, ND, NJ, NV, OH, SD, TX, UT, WI, and WY.
  • Description du dispositif
    Dr. Wischmeier Pack, part numbers: AMS3509 and AMS3509(A || Product packaged in a convenient manner for use in a general clinical procedure
  • 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