{
  "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": "Sterling Heights",
      "state": "MI",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75591",
      "recalling_firm": "Sterling Diagnostics, Inc.",
      "address_1": "36645 Metro Ct",
      "address_2": "N/A",
      "postal_code": "48312-1009",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Domestic: MI    Foreign: Phillipines    VA/DOD: None",
      "recall_number": "Z-0936-2017",
      "product_description": "Urea Nitrogen/Color BUN (Enzymatic Berthelot) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer buys another when kit is consumed.",
      "product_quantity": "131",
      "reason_for_recall": "Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple diagnostic kits due to a recision of the previously  extended expiration dates for the kits.",
      "recall_initiation_date": "20160720",
      "center_classification_date": "20161229",
      "termination_date": "20170322",
      "report_date": "20170104",
      "code_info": "Urea Nitrogen/Color BUN, CAT No. 2290-L     , Lot No. 29051, Expriry: 9/18, Manufactured: 09/21/15"
    }
  ]
}