{
  "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": "Kanata",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86279",
      "recalling_firm": "DNA Genotek Inc.",
      "address_1": "3000-500 Palladium Dr",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution including in the states of CA, MA, MD, MN, NY, PA, and TX. The country of China.",
      "recall_number": "Z-3004-2020",
      "product_description": "PrepIT Q2A Kit, Model PT-Q2A-96 containing component reagent AG (PT-QAG-96) 1.4mL and ST (PT-QST-96) 2.9mL - Product Usage: used for the removal of SDS and other inhibitors from samples collected using DNA Genotek oral sample collection kits.",
      "product_quantity": "74",
      "reason_for_recall": "Reagents were shipped to customers after the  Use by  data indicated on its labeling.",
      "recall_initiation_date": "20200624",
      "center_classification_date": "20200923",
      "termination_date": "20211101",
      "report_date": "20200930",
      "code_info": "Lot PT-Q2A WE11"
    }
  ]
}