{
  "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": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65067",
      "recalling_firm": "Polymer Technology Systems, Inc.",
      "address_1": "7736 Zionsville Rd",
      "address_2": "N/A",
      "postal_code": "46268-2175",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide including Puerto Rico and countries of: UK, CHL, ENG, BEL, ITA, TKY, BEL, LIT, LTV, EGY, SPG, HOK, SWE, MEX, UAE, COR, ISR,  MAL, AUS, POR, POL, SLN and STQ.",
      "recall_number": "Z-1403-2013",
      "product_description": "PTS PANELS, Glucose Test Strips for use with CardioChek Brand Analyzers    Product Usage:  used by healthcare professionals and individuals with diabetes to measure glucose in whole blood",
      "product_quantity": "7048 total, 3499 in USA",
      "reason_for_recall": "Internal investigation demonstrated under-recovery for glucose when tested against a reference method.  This could result in a low to moderate health risk.",
      "recall_initiation_date": "20130404",
      "center_classification_date": "20130524",
      "termination_date": "20140416",
      "report_date": "20130605",
      "code_info": "U1117"
    }
  ]
}