{
  "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": [
    {
      "status": "Terminated",
      "city": "Bristol",
      "state": "CT",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77295",
      "recalling_firm": "Beekley Corporation",
      "address_1": "1 Prestige Ln",
      "address_2": "N/A",
      "postal_code": "06010-7468",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : AR, CA GA, IL, TX, MN, NV, NY, WI., and Internationally to Canada.",
      "recall_number": "Z-2309-2017",
      "product_description": "Beekley Medical 0-SPOT Mammography Skin Markers  REF 652",
      "product_quantity": "104 boxes (58/box)= 6,032 total units",
      "reason_for_recall": "Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels",
      "recall_initiation_date": "20170508",
      "center_classification_date": "20170607",
      "termination_date": "20170620",
      "report_date": "20170614",
      "code_info": "LOT 652.04251701"
    }
  ]
}