Device Recall Stryker inTouch Zoom Critical Care

  • Modèle / numéro de série
    All units. (Model Number 2140/Serial Numbers: T01121, T01205, T01350, T01213 thru T01214, T01224, T01014 thru T01036, T01143, T01227, T01211, T01379 thru T01383, T01202, T01053 thru T01099. T01100 thru T01144, T01159, T01179, T01182, T01378, T01186, T01201, T01212, T01057, T01060,T01079,T01200, T01183, T01189, T01223, T01209, T01218, T01172, T01188, T01058, T01171, T01173, T01195, T01203, T01206, T01210, T01216, T01217, T01228, T01176, T01185, TO1193, T01207, T01225, T01215, T01229, T01187, T01311 thru T01320, T01230, T01175, T01180, T01190, T01196, T01037 thru T01052, T01198, T01184, T01192, T01177, T01194, T01204, T01219, T01199, T01191, T01226, T01181, T01197, T01222, T01231 thru T01308,T01208, T01349, T01221, QT01001 thru QT01012, QT01169 and QT01170)
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide-USA and Canada
  • Description du dispositif
    Stryker inTouch Zoom Critical Care bed, Model 2140, Stryker Medical, Portage, MI 49002
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Stryker Medical Div. of Stryker Corporation, 3800 E. Centre Ave., Portage MI 49002
  • Source
    USFDA