{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Marlborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92357",
      "recalling_firm": "Hologic, Inc",
      "address_1": "250 Campus Dr",
      "address_2": "N/A",
      "postal_code": "01752-3020",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2035-2023",
      "product_description": "Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy samples from soft tissue and tumors of the breast  REF: SERTERA-14",
      "product_quantity": "756 units",
      "reason_for_recall": "The inner needle of the Sertera device is either detaching or discharging and may cause delay in surgery",
      "recall_initiation_date": "20230502",
      "center_classification_date": "20230629",
      "report_date": "20230705",
      "code_info": "UDI-DI: 15420045504066 Lot Number:  E22H19RM",
      "more_code_info": ""
    }
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}