{
  "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": "Bethlehem",
      "state": "PA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87340",
      "recalling_firm": "OraSure Technologies, Inc.",
      "address_1": "220 E 1st St",
      "address_2": "",
      "postal_code": "18015-1360",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of KS, NJ, OH, VA.",
      "recall_number": "Z-1183-2021",
      "product_description": "Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination of methamphetamine in oral fluid, PN 11041C.",
      "product_quantity": "16 units",
      "reason_for_recall": "Incorrect lot of Substrate Reagent (TMB) may be included in the kit. The original kit box labeling and the specification sheet listed the Substrate Reagent (TMB)  lot 6676239, but contained Substrate Reagent (TMB) lot 6679623, should not affect performance.",
      "recall_initiation_date": "20210205",
      "center_classification_date": "20210305",
      "termination_date": "20230330",
      "report_date": "20210317",
      "code_info": "Lot 6681090, Exp date 2021-03.  UDI: 608337000191",
      "more_code_info": ""
    }
  ]
}