{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Cincinnati",
      "address_1": "300 E Business Way Fl 5",
      "reason_for_recall": "The device did not have Revolve Stereo Probe labeling, no product code indicating the size and length of the probe, no sterilization sticker or lot number.",
      "address_2": "",
      "product_quantity": "320",
      "code_info": "F11621304D1",
      "center_classification_date": "20170321",
      "distribution_pattern": "Worldwide Distribution - US including IA, IL, NY, OH, OK, PA, TN & WV.  Internationally to Chile and Brazil",
      "state": "OH",
      "product_description": "Mammotome Revolve Dual Vacuum Assist Biopsy   System  The device is used to sample breast tissue that has been identified as suspicious under imaging guidance",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Devicor Medical Products Inc",
      "recall_number": "Z-1512-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76603",
      "termination_date": "20170803",
      "more_code_info": "",
      "recall_initiation_date": "20170228",
      "postal_code": "45241-2384",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}