{
  "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": [
    {
      "status": "Terminated",
      "city": "Plainsboro",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82361",
      "recalling_firm": "Integra Limited",
      "address_1": "311 Enterprise Dr",
      "address_2": "N/A",
      "postal_code": "08536-3344",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of OH, MI.",
      "recall_number": "Z-1090-2019",
      "product_description": "Integra bioBLOCK Resorbable subtaler Implant, 11mm  Catalog Number: 040011 - Product Usage:   The bioBLOCK Implant is indicated for internal support to primary surgical interventions in the treatment of flatfoot.",
      "product_quantity": "232 total",
      "reason_for_recall": "Temperature indicator may have changed color to dark gray or black prior to shipment. Change in color may indicate the product exposure to temperatures greater than 110¿F",
      "recall_initiation_date": "20190301",
      "center_classification_date": "20190405",
      "termination_date": "20200622",
      "report_date": "20190417",
      "code_info": "Lot Numbers: FGD2096, FGD8328"
    }
  ]
}