{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Naperville",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80110",
      "recalling_firm": "Ekla Corporation",
      "address_1": "1707 Quincy Ave Ste 127",
      "address_2": "",
      "postal_code": "60540-6692",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US National Distribution in the states of CA, IL, MN and  RI",
      "recall_number": "Z-2391-2018",
      "product_description": "NOVAPLUS(R) Pregnancy Cassette Device with Droppers, Urine hCG Pregnancy Cassette, Cat. No. VPT1-CASS    Product Usage:  pregnancy test",
      "product_quantity": "295 kits",
      "reason_for_recall": "Incorrect hCG results",
      "recall_initiation_date": "20161020",
      "center_classification_date": "20180709",
      "termination_date": "20231129",
      "report_date": "20180718",
      "code_info": "Lot # F606032 (exp 2018-05)",
      "more_code_info": ""
    }
  ]
}