{
  "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": "Canton",
      "state": "MI",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77453",
      "recalling_firm": "Medtest Holdings, Inc.",
      "address_1": "5449 Research Dr",
      "address_2": "N/A",
      "postal_code": "48188-2261",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "FL, AR, NICARAGUA, KOREA",
      "recall_number": "Z-2649-2017",
      "product_description": "The Pointe Scientific CK-MB Isoenzyme Control  Pointe Scientific CK-MB Level II Control,  C7562-12 Control Kit",
      "product_quantity": "5 kits",
      "reason_for_recall": "Incorrect control range in product labeling",
      "recall_initiation_date": "20101122",
      "center_classification_date": "20170629",
      "termination_date": "20170724",
      "report_date": "20170705",
      "code_info": "Model C7562-12 Control Kit.  Lot: 013206-260, Expiration Date: 2013-03"
    }
  ]
}