{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Franklin Lakes",
      "address_1": "509 Commerce St",
      "reason_for_recall": "On 8/25/2015, Collagen Matrix, Inc discovered that one of the 171 units of NuOss Cancellous product shipped to a distributor may have included an incorrect size.",
      "address_2": "",
      "product_quantity": "171 units",
      "code_info": "Reference No. BM2C20010-U  Lot no. BM2CU15E2",
      "center_classification_date": "20160311",
      "distribution_pattern": "US Distribution to the state of : MA",
      "state": "NJ",
      "product_description": "NuOSS Cancellous    Intended for use in dental surgery.",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Collagen Matrix Inc",
      "recall_number": "Z-1096-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73222",
      "termination_date": "20160511",
      "more_code_info": "",
      "recall_initiation_date": "20150825",
      "postal_code": "07417-1374",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}