Device Recall Rebound Air Walker

  • Model / Serial
    Item No: B-242900001 B-242900001E B-242900001SE B-242900002 B-242900002E B-242900002SE B-242900003 B-242900003E B-242900003SE B-242900004 B-242900004E B-242900004SE B-242900005 B-242900005E B-242900005SE B-242900061 B-242900061E B-242900061SE B-242900062 B-242900062E B-242900062SE B-242900063 B-242900063E B-242900063SE B-242900064 B-242900064E B-242900064SE B-242900065 B-242900065E B-242900065SE
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    U.S. distribution to the following; AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, RI, TN, TX, UT, VA, VT, WA, WI, WV
  • Product Description
    Rebound Air Walker || Product Usage: || Rebound Air Walkers are indicated for grade 2 and grade 3 ankle sprains, to stabilize fractures, post-operative use, and trauma or rehab use.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Ossur H / F, Grjothals 5, Reykjavik Iceland
  • Manufacturer Parent Company (2017)
  • Source
    USFDA