{
  "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": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "9940 Mesa Rim Rd",
      "reason_for_recall": "Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX LOT #188744)",
      "address_2": "",
      "product_quantity": "3400 units (136 kits)",
      "code_info": "Catalog Number:  QT11  Lot Number: 188787",
      "center_classification_date": "20191217",
      "distribution_pattern": "US - AZ, CA, FL, GA, KS, LA, MI, MO, MS, NC, OK, TN, and TX.    OUS - None",
      "state": "CA",
      "product_description": "QuickTox 5 Panel Drug Screen DipCard",
      "report_date": "20191225",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Ameditech Inc",
      "recall_number": "Z-0692-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "84239",
      "termination_date": "20210428",
      "more_code_info": "",
      "recall_initiation_date": "20190215",
      "postal_code": "92121-2910",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}