Device Recall Hand Foot II

  • Modelo / Serial
    Serial numbers: 39870, 39873, 39874, 39866, 39867, 39871, 39869
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    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.
  • Descripción del producto
    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

Fabricante

  • Dirección del fabricante
    National Biological Corp, 23700 Mercantile Rd, Beachwood OH 44122-5900
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA