{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79549",
      "recalling_firm": "Ameditech Inc",
      "address_1": "9940 Mesa Rim Rd",
      "address_2": "N/A",
      "postal_code": "92121-2910",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed domestically to AZ, FL, IL, ND, NV, PA, TN, TX, VA.",
      "recall_number": "Z-1542-2018",
      "product_description": "Alere iScreen Dx Urine Drug Screen Card",
      "product_quantity": "828 kits (20,700 devices)",
      "reason_for_recall": "The kit box label incorrectly identifies Phencyclidine (PCP), where it should list Tricyclic Antidepressants (TCA) as one of the 10 drug analytes included in the kit box.",
      "recall_initiation_date": "20171215",
      "center_classification_date": "20180428",
      "termination_date": "20190211",
      "report_date": "20180509",
      "code_info": "Part No. X11-IS10-Dx, Lot No. 173351, 173686, 174055, 176002."
    }
  ]
}