{
  "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": "77445",
      "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": "Nationwide Distribution",
      "recall_number": "Z-2650-2017",
      "product_description": "Pointe Scientific Liquid Creatine Kinase Reagent Set  Device is a kit comprised of two reagents an R 1 Buffer and R2 CK enzyme solution. Intended Use: For the kinetic quantitative determination of creatine kinase activity in serum.",
      "product_quantity": "319.922 L",
      "reason_for_recall": "Linear performance information in product insert does not match that listed in the approved premarket notification",
      "recall_initiation_date": "20111019",
      "center_classification_date": "20170629",
      "termination_date": "20170724",
      "report_date": "20170705",
      "code_info": "Models: C7522, HC422, HC722, HC922.  Lot#'s: 020902; 029902 R1; 029902 R2; 029903; 113204; 129403; 209001.  Exp dates 7/2012 to 9/2013."
    }
  ]
}