Bock,Otto,Orthopedic Ind,Inc

2 devices in the database

  • Model / Serial
    The affected strollers were sold between August 1, 2002 and September 23, 2003. The affected strollers are those strollers equipped with the trigger-activated tilting mechanism. (The firm''s notification letter has photographs of the trigger-activated tilting mechanism which can be used to identify the devices needing correction.)
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    The product was distributed nationwide in the United States and to Canada and Mexico.
  • Product Description
    Otto Bock Kimba Plus Pediatric Tilt-in-Space Postural Mobility Systems (Strollers), Product Numbers HR32571001-012, HRK3269=06-027_X, R32651001-012, HRK3283=01-026_X, HRK3269=01-026_X, HRK3283=02-026_X, HRK3269=02-026_X, HRK3283=03-027_X, HRK3269=03-027_X, HRK3283=04-027_X, HRK3269=04-027_X, HRK3283=05-026_X, HRK3269=05-026_X, and HRK3283=06-027_X
  • Model / Serial
    No lot numbers are used. Recall covers patients who were fit with either of the products between March 1, 2004 and July 9, 2004.
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Product Description
    Modular Knee Joint with Friction Brake

One manufacturer with a similar name

Learn more about the data here

  • Manufacturer Address
    Bock,Otto,Orthopedic Ind,Inc, Two Carlson Parkway North, Suite 100, Minneapolis MN 55447
  • Source
    USFDA