{
  "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": "Sunrise",
      "address_1": "1560 Sawgrass Corporate Pkwy",
      "reason_for_recall": "Presence of one inoperable (dead) sensor pad.",
      "address_2": "4th Floor",
      "product_quantity": "22 devices",
      "code_info": "Model SYK-TRCR 02, Lot # 091914V11770, Serial #s: 411654008, 411585023, 411654007, 411585032, 411585014, 411654016, 411585017, 411654015, 411585030, 411654020, 411654004, 411654010, 411585007, 411585005, 411654011, 411585036, 411585035, 411654018, 411654012, 411585011, 411654014, 411654005, 411654001, 411585003.",
      "center_classification_date": "20150129",
      "distribution_pattern": "US Distribution to the states of : IL, MI, NY, CA, VA and NV.",
      "state": "FL",
      "product_description": "Verasense Knee System, Model SYK-TRCR 02.  Intelligent disposable tibial insert that measures dynamic loads during orthopedic knee surgery.",
      "report_date": "20150204",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Orthosensor, Inc.",
      "recall_number": "Z-1029-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69963",
      "termination_date": "20150313",
      "recall_initiation_date": "20141205",
      "postal_code": "33323-2858",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}