Device Recall Bevel Single Shot Needle

  • Modèle / numéro de série
    20130220, 20130527, 20130610, 5066234837, 5122261794, 5206296119, 5325344651, 6088396272, 6129418992, 6160431977, 6174438865, 6194446416, 6226460919, 6235463674, 6268479139, 7059551764, 7074559184, 7107573676, 7143590429, 7176604915, 7192611055, 7240632670, 8105738005, 8177772497, 8203783809, 8240801366, 8277818568 and 8302830746.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution: United States, including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, and UT.
  • Description du dispositif
    21G x 90mm/45 Bevel Single Shot Needle, REF 554-021-090, Rx, Sterile, Distributed by: Stryker Instruments, Kalamazoo, MI.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Stryker Instruments Div. of Stryker Corporation, 4100 E. Milham Ave., Kalamazoo MI 49001
  • Société-mère du fabricant (2017)
  • Source
    USFDA