{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70668",
      "recalling_firm": "Lusys Laboratories, Inc.",
      "address_1": "10054 Mesa Ridge Ct Ste 118-120",
      "address_2": "N/A",
      "postal_code": "92121-2946",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US including CA and Internationally to Canada, Sierra Leone, and Denmark.",
      "recall_number": "Z-1330-2015",
      "product_description": "Ebola VP-40 IgG/IgM (Blood Serum/Plasma/Cassette), Catalog No. I-102    Materials Provided:  1. Test Device   2. Lancet (optional)   3. Alcohol pad. (optional)   4. Extraction tube (optional)   5. Buffer vial (0.5ml) --- packaged",
      "product_quantity": "80 units",
      "reason_for_recall": "LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and prevent further use of these devices.  The Ebola Virus One-Step Test Kits have not yet been cleared, approved or authorized by the FDA for diagnostics purposes.",
      "recall_initiation_date": "20150313",
      "center_classification_date": "20150409",
      "termination_date": "20170531",
      "report_date": "20150415",
      "code_info": "Lot No. 11192014B"
    }
  ]
}