Device Recall Eye Pack

  • Modèle / numéro de série
    Lot numbers:   62736 63388 63389 64189 64190 64586 65070 65171 65307 65714 65715 66342 66343 67079 67080 68165 68166 68234 68641 69264 69536 69545
  • 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
    Eye Pack, part numbers WAL1085(B and WAL1085(C\ || 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