{
  "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": "Santa Clarita",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83820",
      "recalling_firm": "TriMed Inc.",
      "address_1": "27533 Avenue Hopkins",
      "address_2": "N/A",
      "postal_code": "91355-3910",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was nationwide.  There was military distribution but no government distribution.  Foreign distribution was made to Australia, China, South Africa, and Sweden.",
      "recall_number": "Z-0357-2020",
      "product_description": "TriMed Hex Driver 1.2, 55mm AO Cannulated, REF HXDRIVR-1.2C AO, nonsterile, Rx.  The firm name on the label is TriMed Inc., Santa Clarita, CA.",
      "product_quantity": "467 hex drivers",
      "reason_for_recall": "The epoxy on Apex manufactured epoxy-coated instruments can pop off.",
      "recall_initiation_date": "20180928",
      "center_classification_date": "20191112",
      "report_date": "20191120",
      "code_info": "Lot numbers 91500604 and 91600017"
    }
  ]
}