{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Canton",
      "address_1": "5449 Research Dr",
      "reason_for_recall": "Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set stability claim is not being met.",
      "address_2": "",
      "product_quantity": "716.146L total",
      "code_info": "L7572 all configurations",
      "center_classification_date": "20170526",
      "distribution_pattern": "Nationwide",
      "state": "MI",
      "product_description": "Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set   Model Number(s): L7572.    For the in vitro quantitative kinetic determination of lactate dehydrogenase activity in serum.",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtest Holdings, Inc.",
      "recall_number": "Z-2165-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "77048",
      "termination_date": "20170602",
      "more_code_info": "",
      "recall_initiation_date": "20110708",
      "postal_code": "48188-2261",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}