{
  "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": "Scottsdale",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88281",
      "recalling_firm": "Advance Dx, Inc.",
      "address_1": "11250 N 118th Way",
      "address_2": "N/A",
      "postal_code": "85259-4149",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of MD and NC.",
      "recall_number": "Z-2237-2021",
      "product_description": "Advance Dx 100 Blood Collection Card Quantity 25  REF CMT01    Advance Dx 100 Blood Collection Card and Foil Bags Quantity 500 Cards and Foil Bags  REF CMT01/F02    IFU:  Advance Dx 100 SSE(Serum Separating Extraction) Technology  BLOOD COLLECTION INSTRUCTIONS",
      "product_quantity": "179,750 cards",
      "reason_for_recall": "Due to high glucose test results when using the blood collection cards.",
      "recall_initiation_date": "20210706",
      "center_classification_date": "20210810",
      "termination_date": "20230822",
      "report_date": "20210818",
      "code_info": "Product Catalog Number: CMT01 GTIN: 1061C010890976 Lot Number: PPD02102 V6"
    }
  ]
}