{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Titusville",
      "address_1": "1125 Trenton-Harbourton Rd.",
      "reason_for_recall": "Labeling: Incorrect Instructions; Instructions included  for use with the Veridate dispenser contained instructions for the Dialpak dispenser.",
      "address_2": "",
      "product_quantity": "1,777 cartons",
      "code_info": "Lot # 18BM114, Exp. 03/2020",
      "center_classification_date": "20181106",
      "distribution_pattern": "Nationwide in the USA",
      "state": "NJ",
      "product_description": "Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets, 1 mg/0.035 mg, 28-Day Regimen per pouch (NDC 50458-176-28), 6 Veridate Tablet Dispensers and 6 refills per carton (NDC 50458-176-06), Rx only, Manufactured by: Janssen Ortho, LLC, Manati, Puerto Rico 00674; Manufactured for: Janssen Pharmaceuticals, Inc., Titusville, New Jersey 08560.",
      "report_date": "20181114",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Janssen Pharmaceuticals, Inc.",
      "recall_number": "D-0217-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "81289",
      "termination_date": "20191030",
      "more_code_info": "",
      "recall_initiation_date": "20181023",
      "postal_code": "08560",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}