Device Recall STRYKER CASSETTE PUMP, AHTO Tube Set

  • Modèle / numéro de série
    a. Model 0250070600, UDI 07613327061499, Lot No. 17284FG2, 17291FG2, 17300FG2;  b. Model 0250070620, UDI 07613327061659, Lot No. 17275FG2, 17279FG2, 17280FG2, 17282FG2, 17283FG2, 17284FG2, 17285FG2, 17286FG2, 17289FG2, 17291FG2, 17292FG2, 17293FG2, 17297FG2, 17298FG2, 17299FG2;
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed domestically to . Distributed internationally to Australia and Mexico.
  • Description du dispositif
    STRYKER CASSETTE PUMP, AHTO Tube Set, labeled sterile. Includes the following: || a. Stryker AHTO Tube Set Packaging (Model 0250070600); || b. Stryker AHTO Tube Set with Tip Packaging (Model 0250070620);
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Stryker Corporation, 5900 Optical Ct, San Jose CA 95138-1400
  • Société-mère du fabricant (2017)
  • Source
    USFDA