{
  "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": "2026-06-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cincinnati",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98843",
      "recalling_firm": "Devicor Medical Products Inc",
      "address_1": "300 E Business Way Fl 5",
      "address_2": "",
      "postal_code": "45241-2384",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Singapore.",
      "recall_number": "Z-2239-2026",
      "product_description": "HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3",
      "product_quantity": "1910 units",
      "reason_for_recall": "Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.",
      "recall_initiation_date": "20260424",
      "center_classification_date": "20260527",
      "report_date": "20260603",
      "code_info": "Lot Number: F12607207D",
      "more_code_info": ""
    }
  ]
}