Device Recall 27023WU Balloon Catheter

  • Modèle / numéro de série
    Lots: 12471, 12281, 12271, 12171, 12101, 12051, 11501, 11401, 09471, 09431, 09251, 09201, 09161, 09091, 09071, 08451.
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    US distribution to: AZ, FL, IL, IN and TX.
  • Description du dispositif
    27023WU Balloon Catheter, 3 Fr., 2/pkg, sterile, contains latex. || The RUSCH ureter occlusion catheter is indicated for the routine occlusion of the ureter to prevent the movement of stone fragments during treatment. The coaxial catheters will also allow simultaneous drainage of urine or infusion of other solutions.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Karl Storz Endoscopy America Inc, 15 Wells St, Southbridge MA 01550-4503
  • Société-mère du fabricant (2017)
  • Source
    USFDA