{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98709",
      "recalling_firm": "Quidel Corporation",
      "address_1": "10165 McKellar Ct",
      "address_2": "",
      "postal_code": "92121-4201",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, FL, ID, IL, LA, MA, MD, MN, MO, NY, PA, SC, TN, TX, VA.",
      "recall_number": "Z-2169-2026",
      "product_description": "QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.",
      "product_quantity": "12279 units",
      "reason_for_recall": "Product has the potential for false positive results",
      "recall_initiation_date": "20260406",
      "center_classification_date": "20260512",
      "report_date": "20260520",
      "code_info": "UDI/DI 30014613201083, Lot Numbers:  225788, 228322, 233274.",
      "more_code_info": ""
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}