{
  "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": [
    {
      "status": "Terminated",
      "city": "Beaumont",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83622",
      "recalling_firm": "Helena Laboratories, Corp.",
      "address_1": "1530 Lindbergh Dr",
      "address_2": "N/A",
      "postal_code": "77707-4131",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Distribution was made to IN, KY,  MA, OH, OR, TN, and TX.  There was government distribution.  Foreign distribution was made to Chile.",
      "recall_number": "Z-0045-2020",
      "product_description": "SPIFE ImmunoFix-6 Kit, Cat. No. 3401, 3401T, For In-Vitro Diagnostic Use.  The firm name on the label is Helena Laboratories, Beaumont, TX.",
      "product_quantity": "24 kits",
      "reason_for_recall": "The plates do not have wells punched for the controls in the patient 1 area.",
      "recall_initiation_date": "20170721",
      "center_classification_date": "20191004",
      "termination_date": "20200619",
      "report_date": "20191016",
      "code_info": "Lot 35-17-552583, exp. date 4/30/2018"
    }
  ]
}