{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "700 Orthopaedic Dr",
      "reason_for_recall": "The device will not connect to the Specialist 2 Locating Outrigger which renders them unusable in surgery.",
      "address_2": "",
      "product_quantity": "140 total units",
      "code_info": "Lot SO2040929  ***Updated 7/9/20***  Lot SO2040602  Lot SO2037408 (None of this lot distributed in the US / OUS distribution only)",
      "center_classification_date": "20200212",
      "distribution_pattern": "Domestic distribution to IA, MA, NY, OH, and PA. Foreign distribution to Canada, China, Hungary, United Kingdom, and Singapore. ***Updated 7/9/20*** Expanded notice includes 6 new countries: Belgium, France, Germany, Maldives, New Zealand, and UAE",
      "state": "IN",
      "product_description": "SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115.    The product is a femoral cutting block.",
      "report_date": "20200219",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "DePuy Orthopaedics, Inc.",
      "recall_number": "Z-1169-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84714",
      "termination_date": "20210812",
      "more_code_info": "",
      "recall_initiation_date": "20200103",
      "postal_code": "46582-3994",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}