{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86335",
      "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": "US - Nationwide  OUS - Australia, France, Germany, New Zealand, Singapore and Spain",
      "recall_number": "Z-3033-2020",
      "product_description": "Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Description):    164-DXA14 /\"Consult Diagnostics  DRUGS OF ABUSE TEST CUP 14-DRUG PANEL WITH ADULTERANTS  AMP500/BAR/BUPG/BZO/COC150/MDMA/MET500/MOP/MTD/OXY/PCP/PPX/TCA/THC (Bl, Cr, Ni, pH, SG)\",",
      "product_quantity": "31,600 units",
      "reason_for_recall": "Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.",
      "recall_initiation_date": "20200818",
      "center_classification_date": "20200930",
      "termination_date": "20240930",
      "report_date": "20201007",
      "code_info": "ALL Lots Within Expiry"
    }
  ]
}