{
  "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": "Terminated",
      "city": "Redwood City",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82763",
      "recalling_firm": "AURIS HEALTH INC",
      "address_1": "150 Shoreline Dr",
      "address_2": "N/A",
      "postal_code": "94065-1400",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution to the states of: CT, FL, MI, OK, TN, MS, CA, MN, OH, PA, and IL.",
      "recall_number": "Z-0025-2020",
      "product_description": "Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120",
      "product_quantity": "158",
      "reason_for_recall": "Reports of aspirating biopsy needle breakage",
      "recall_initiation_date": "20190419",
      "center_classification_date": "20191115",
      "termination_date": "20220119",
      "report_date": "20191127",
      "code_info": "Lots:   RS181129-1  RS181129-2  RS181210-1  RS181210-2  RS181210-3  RS181210-4  RS190117-1  RS190125-1  RS190211-1  RS190225-3  RS190308-1  RS190319-1"
    }
  ]
}