{
  "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-0359-2020",
      "product_description": "TriMed Wrist Hook Dorsal Impactor, REF IMPCT-WHD; and TriMed Wrist Hook Volar Impactor, REF IMPCT-WHV, both nonsterile, Rx,  The firm name on the labels is TriMed Inc., Santa Clarita, CA.",
      "product_quantity": "561 devices",
      "reason_for_recall": "The WHD/WHV impactors can rust over time due to an improper manufacturing process.",
      "recall_initiation_date": "20180928",
      "center_classification_date": "20191112",
      "report_date": "20191120",
      "code_info": "Lot numbers 049045, 049044, and 049044R1."
    }
  ]
}