{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91419",
      "recalling_firm": "Carbon Medical Technologies, Inc.",
      "address_1": "1290 Hammond Rd",
      "address_2": "N/A",
      "postal_code": "55110-5867",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of OHIO.",
      "recall_number": "Z-1041-2023",
      "product_description": "Mammotome MammoStar Biopsy Site Identified, REF STAR1401",
      "product_quantity": "550 devices",
      "reason_for_recall": "The label incorrectly identifies the product as STAR1401, a 1x3mm Barbell shaped marker pre-loaded in a 14 gauge needle, while the packaging contains STAR1402, a 1x5mm Tribell shaped marker pre-loaded in a 14 gauge needle.",
      "recall_initiation_date": "20221216",
      "center_classification_date": "20230130",
      "termination_date": "20230809",
      "report_date": "20230208",
      "code_info": "UDI/DI 00858015005431, Lot Number 2201011A"
    }
  ]
}