{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Burlington",
      "state": "NC",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "61737",
      "recalling_firm": "Tripath Imaging, Inc.",
      "address_1": "780 Plantation Dr",
      "address_2": "N/A",
      "postal_code": "27215-6723",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution.",
      "recall_number": "Z-1813-2012",
      "product_description": "PrepStain Installation Kit (PreCoat), Catalog/Model # 490528",
      "product_quantity": "46,112,784 for all products in Recall Event",
      "reason_for_recall": "The PrepStain Syringing Pipettes may not dispense the minimum volume of 7.5 mL of the sample due to leaking. This event resulted in an increase in complaints of leaking syringing pipettes",
      "recall_initiation_date": "20120322",
      "center_classification_date": "20120615",
      "termination_date": "20121203",
      "report_date": "20120627",
      "code_info": "100917ry, 101105sh, 110107rg"
    }
  ]
}