Stic Kit Needle Containment Device

  • Modelo / Serial
    The recalled units are identified with the Lot Codes: 070505 and 110602.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The recalled device was shipped to distributor/customers located in the following states: MO, OH, WI, PA and NJ.
  • Descripción del producto
    Model EMI 82691, Stic Kit Needle Containment Device. These devices are packaged 60 per case. Stick-on label on device and User Instruction sheet are attached to the case with a rubber band.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    EM Innovations Inc, 6106 Bausch Rd, Galloway OH 43119-9382
  • Source
    USFDA