{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Cincinnati",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90119",
      "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": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of DE, KY, NY, OH, WV.",
      "recall_number": "Z-1124-2022",
      "product_description": "HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4",
      "product_quantity": "90 devices",
      "reason_for_recall": "Small patient labels do not match the primary device label. The primary device label accurately identifies the product as 4010-05-08-T4, while the smaller patient label  incorrectly identifies the product as 4010-05-08-T3.",
      "recall_initiation_date": "20220330",
      "center_classification_date": "20220523",
      "termination_date": "20240430",
      "report_date": "20220601",
      "code_info": "UDI-DI: 00841911102472 Lot F12201281D",
      "more_code_info": ""
    }
  ]
}