Device Recall Synthes(R) Hemostatic Bone Putty

  • Modèle / numéro de série
    All lot numbers associated with the identified part numbers.
  • Classification du dispositif
  • Classe de dispositif
    Unclassified
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution -- US, including Washington, DC and states of AK, AZ, CA, CT, FL, GA, ID, KS, LA, MD, MA, MI, MN, MO, NE, NH, NY, NC, OH, OR, PA, SC, TX, VA, WA, and WI, and the country of Canada.
  • Description du dispositif
    Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.901.001D, and VB1025.10S. || Indicated for use as a water soluble implant material and for use in the control of bleeding from bone surfaces.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Synthes USA HQ, Inc., 1302 Wrights Ln E, West Chester PA 19380-3417
  • Société-mère du fabricant (2017)
  • Source
    USFDA