Device Recall Hand Foot II

  • Modèle / numéro de série
    Serial numbers: 39870, 39873, 39874, 39866, 39867, 39871, 39869
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution. US states: IA, IL, MI, NY, PA, and WI. Country: Jordan. There are no government accounts for this recall. There are no Canada accounts for this recall. There are no Mexico accounts for this recall.
  • Description du dispositif
    Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    National Biological Corp, 23700 Mercantile Rd, Beachwood OH 44122-5900
  • Société-mère du fabricant (2017)
  • Source
    USFDA