{
  "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": "Medford",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86098",
      "recalling_firm": "Chembio Diagnostics, Inc",
      "address_1": "3661 Horseblock Rd",
      "address_2": "N/A",
      "postal_code": "11763-2215",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-2808-2020",
      "product_description": "Chembio DPP¿ Micro Reader for use with the DPP¿ COVID-19 IgM/IgG System- Rapid immunochromatographic test for the qualitative detection and differentiation of Immunoglobulin M (IgM) and Immunoglobulin G (IgG) antibodies to SARS-CoV-2 in fingerstick whole blood, venous whole blood, serum, or plasma (lithium heparin or EDTA. Model Number: 70-1069-0",
      "product_quantity": "126 kits",
      "reason_for_recall": "FDA revocation of the Emergency Use Authorization due to performance issues",
      "recall_initiation_date": "20200618",
      "center_classification_date": "20200814",
      "termination_date": "20210811",
      "report_date": "20200826",
      "code_info": "Lot Numbers:  83716171  83720151  83720153"
    }
  ]
}