{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allendale",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85400",
      "recalling_firm": "Howmedica Osteonics Corp.",
      "address_1": "2 Pearl Ct",
      "address_2": "N/A",
      "postal_code": "07401-1611",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to California  Colorado  Florida  Georgia  Illinois  Indiana  Kansas  Michigan  Ohio  Pennsylvania  Texas  Utah  Virginia  Washington  Wisconsin",
      "recall_number": "Z-1900-2020",
      "product_description": "Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010",
      "product_quantity": "115",
      "reason_for_recall": "Shipments were transported outside of the required refrigerated temperature conditions. Potential hazards if used include nerve damage resulting in paralysis and increased potential for embolism.",
      "recall_initiation_date": "20200401",
      "center_classification_date": "20200505",
      "termination_date": "20200827",
      "report_date": "20200513",
      "code_info": "Specific shipments of 2101-0005: Lots A1907006, A1908003;  2101-0010: Lots A1903054, A1906006.   UDI 00808232000962, 00808232000979",
      "more_code_info": ""
    }
  ]
}