{
  "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": "Ongoing",
      "city": "San Antonio",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92390",
      "recalling_firm": "New Standard Device Inc",
      "address_1": "4848 Research Dr",
      "address_2": "N/A",
      "postal_code": "78240-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S. Nationwide distribution in the states of AZ, CT, OH, TX, VA.",
      "recall_number": "Z-1824-2023",
      "product_description": "'n'-Hole Post which is a component of the Revolution External Fixation System    Catalog Numbers:  100801,  100802,  100803,  100804,  100805",
      "product_quantity": "222 units",
      "reason_for_recall": "The threads on posts stripping out when tensioned during application process.",
      "recall_initiation_date": "20190723",
      "center_classification_date": "20230609",
      "report_date": "20230621",
      "code_info": "Catalog Numbers / Lot Numbers: 100801 / A29318R 100802 / A29318S 100803 / A29318T 100804 / A29318U 100805 / A29318V  UDI Codes: Not provided/None"
    }
  ]
}