{
  "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": [
    {
      "country": "United States",
      "city": "Hillsboro",
      "address_1": "5885 NW Cornelius Pass Rd",
      "reason_for_recall": "OPT Croutons, part number 65-0210-S, is recalled due to the result of inadequate documentation of the sterilization dose used in production. Product sterilized at the site did not receive the minimum dose required per the new performance qualification.",
      "address_2": "",
      "product_quantity": "83 units distributed in the US",
      "code_info": "lot 549/12.001.  Part number 65-0210-S.",
      "center_classification_date": "20170112",
      "distribution_pattern": "distributed in FL, IN, KS, MI, MO, NE, OH, PA, TX and Peurto Rico.",
      "state": "OR",
      "product_description": "OPT Croutons is a synthetic bone substitute designed for the repair of bony defects and is made of pure beta-tricalcium phosphate. The tricalcium phosphate is a soluble calcium phosphate salt.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Acumed LLC",
      "recall_number": "Z-1019-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75904",
      "termination_date": "20170322",
      "more_code_info": "",
      "recall_initiation_date": "20161205",
      "postal_code": "97124-9432",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}