{
  "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,
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  "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-3047-2020",
      "product_description": "First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B",
      "product_quantity": "47,005 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"
    }
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}