{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Arlington",
      "address_1": "5677 Airline Rd",
      "reason_for_recall": "ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening.",
      "address_2": "",
      "product_quantity": "47 units",
      "code_info": "all codes",
      "center_classification_date": "20160908",
      "distribution_pattern": "Worldwide Distribution only to Australia, Austria, France, Italy, Spain, and United Kingdom",
      "state": "TN",
      "product_description": "ADVANCE(R) II MODULAR TIBIAL BASE W/SCREWHOLES, Knee Tibial Base,  REF KTTIHA51, SIZE 5+; SURFACE POROUS, HA COATED; FIT CEMENTLESS; USE W/ SIZE 5 FEMUR & SIZE 5 TIBIAL INSERT; CONTENTS, 1 EACH, STERILE R, Rx ONLY, MicroPort Knee Systems Total Knee Systems MicroPort Total Knee Systems are indicated for use in knee arthroplasty in skeletally mature patients with the following conditions: 1) noninflammatory degenerative joint disease including osteoarthritis, traumatic arthritis, or avascular necrosis; 2) inflammatory degenerative joint disease including rheumatoid arthritis; 3) correction of functional deformity; 4) revision procedures where other treatments or devices have failed; and treatment of fractures that are unmanageable using other techniques.",
      "report_date": "20160914",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "MicroPort Orthopedics Inc.",
      "recall_number": "Z-2702-2016",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "74785",
      "termination_date": "20170726",
      "more_code_info": "",
      "recall_initiation_date": "20160621",
      "postal_code": "38002-9501",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}