{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Indianapolis",
      "address_1": "7736 Zionsville Rd",
      "reason_for_recall": "This lot of test strips is showing an under-recovery when tested against a reference method.",
      "address_2": "",
      "product_quantity": "6467",
      "code_info": "Lot Number I502, UDI 00381932412018",
      "center_classification_date": "20191226",
      "distribution_pattern": "The products were distributed to the following US states:  CA, CT, FL, IN, MA, MD, MI, MN, NC, NJ, NM, NY, OR, PA, TN, and WI.    The products were distributed to the following foreign countries:  Australia, Belgium, Indonesia, Italy, Poland, South Africa, UK, and Vietnam.",
      "state": "IN",
      "product_description": "PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers",
      "report_date": "20200101",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Polymer Technology Systems, Inc.",
      "recall_number": "Z-0741-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84264",
      "termination_date": "20200605",
      "more_code_info": "",
      "recall_initiation_date": "20160315",
      "postal_code": "46268-2175",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}