{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81951",
      "recalling_firm": "OMNIlife science Inc.",
      "address_1": "480 Paramount Dr",
      "address_2": "N/A",
      "postal_code": "02767-1085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "The products were distributed to the following US states:  CA, GA, SC, and UT.",
      "recall_number": "Z-0837-2019",
      "product_description": "OMNI K1 Broach Handle, Product Code HS-10054",
      "product_quantity": "7",
      "reason_for_recall": "There is a potential for the inner pin of the handle to become loose and fall out.",
      "recall_initiation_date": "20181129",
      "center_classification_date": "20190214",
      "termination_date": "20200416",
      "report_date": "20190220",
      "code_info": "Lot Number MM0118"
    }
  ]
}