{
  "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": "Bristol",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62526",
      "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 Nationwide Distribution",
      "recall_number": "Z-2112-2012",
      "product_description": "Beekley Altus Floral Skin Markers -Order Number: 754    Product Usage:  designed for Digital Mammography-Disposable skin markers for marking  areas of concern or pain",
      "product_quantity": "6420 units",
      "reason_for_recall": "Digital Skin Mammography Marker  separating from the backing of the spot material",
      "recall_initiation_date": "20120709",
      "center_classification_date": "20120730",
      "termination_date": "20130709",
      "report_date": "20120808",
      "code_info": "Lot Numbers:   A004"
    }
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}