{
  "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": "2026-04-01",
    "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": "82331",
      "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": "Domestic distribution nationwide.",
      "recall_number": "Z-1371-2019",
      "product_description": "Lipid Panel test strips, REF 1710, also private labeled under Henry Schein as REF 570-0414",
      "product_quantity": "67643 total",
      "reason_for_recall": "Some lots of test strips do not fit tightly into the optical block, and may fall out during analysis, which could lead to an incorrect result being displayed.",
      "recall_initiation_date": "20190116",
      "center_classification_date": "20190523",
      "termination_date": "20200624",
      "report_date": "20190529",
      "code_info": "P832"
    }
  ]
}