{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Irvington",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71127",
      "recalling_firm": "MELA Sciences, Inc.",
      "address_1": "50 S Buckhout St Ste 1",
      "address_2": "N/A",
      "postal_code": "10533-2204",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "AL, CA, CT, CO, FL, HI, IL, MA, MD, MI, NH, NJ, NY, OH, PA, RI, SC, TN, TX, VA and WA",
      "recall_number": "Z-1636-2015",
      "product_description": "MelaFind Device, Model MF 100 US, optical diagnostic device for melanoma detection.",
      "product_quantity": "65 units",
      "reason_for_recall": "The probability and histogram data within the Melafind's device displayed user interface lacks approval (not included in the PMA supplement).",
      "recall_initiation_date": "20150402",
      "center_classification_date": "20150520",
      "termination_date": "20160504",
      "report_date": "20150527",
      "code_info": "UDI   *+M709MF100US0/$$+7DN0123MAS*"
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}