{
  "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
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Brea",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85229",
      "recalling_firm": "Carolina Liquid Chemistries Corp",
      "address_1": "510 W Central Ave Ste C",
      "address_2": "N/A",
      "postal_code": "92821-3032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S.: NC, TX, FL, NY, AZ, NJ, NH, CA",
      "recall_number": "Z-1743-2020",
      "product_description": "Fentanyl Reagent Kit, Product N. CC444, Contains: FENT R1 Reagent and FENT R2 Reagent",
      "product_quantity": "90 test kits/devices",
      "reason_for_recall": "Labeled for diagnostic use and sold to clinical labs without a 510(k).  Firm corrected labeling to remove clinical diagnostic language and notified customers that products are labeled for \"Forensic Use Only\" and are not FDA Cleared and not to be used for clinical purposes",
      "recall_initiation_date": "20200120",
      "center_classification_date": "20200417",
      "termination_date": "20210114",
      "report_date": "20200429",
      "code_info": "Lots: H1801, C1942, D1945, H1901, H1933, L1909"
    }
  ]
}