{
  "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": "Fremont",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74861",
      "recalling_firm": "Microgenics Corporation",
      "address_1": "46500 Kato Rd",
      "address_2": "N/A",
      "postal_code": "94538-7310",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) to states of: AZ, CA, MO, TX, and PR  and countries of: Canada, Germany, Hong Kong, Italy, Malaysia, and Taiwan.",
      "recall_number": "Z-2884-2016",
      "product_description": "DRI Salicylate Serum Tox Assay, Catalog number 0977.    Toxicology:  The DRI Salicylate Serum Tox Assay is intended for the quantitative determination of salicylate in human serum or plasma.",
      "product_quantity": "1708 kits",
      "reason_for_recall": "Some lots of DRI Salicylate Serum Tox Assay negative patient samples are recovering higher than the product sensitivity claim of 4.4 mg/dL.",
      "recall_initiation_date": "20160725",
      "center_classification_date": "20160923",
      "termination_date": "20161121",
      "report_date": "20161005",
      "code_info": "Lot Number      Expiration Date  60704602         DEC 2016;  72035410         JUL 2017;  72208738          FEB 2018;  72409454          OCT 2018."
    }
  ]
}