Device Recall wheeled adult and junior walkers

  • Modèle / numéro de série
    All 6240-5F and 6240-JR5F wheeled walkers distributed by the firm between 12/15/2010 and 3/4/2011, are subject to recall/correction.
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide: AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, including Puerto Rico and countries of Canada, Columbia, and Israel.
  • Description du dispositif
    Dual Blue-Release Adult Walkers - Wheeled, and Blue Release Junior Walkers with 5 inch Fixed Wheels, Model Numbers: 6240-5F and 6240-JR5F. The recalled product is packaged four (4) units per shipping box. || Product Usage: The walkers are intended for people who need additional support to maintain balance or stability while walking.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Invacare Corporation, 1200 Taylor St, Elyria OH 44035-4190
  • Société-mère du fabricant (2017)
  • Source
    USFDA