{
  "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": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89161",
      "recalling_firm": "Tapemark Company",
      "address_1": "1685 Marthaler Ln",
      "address_2": "N/A",
      "postal_code": "55118-3517",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of CA, FL, IL, MO, NY, OH, and TN.",
      "recall_number": "Z-0454-2022",
      "product_description": "iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery System,  Extra Strength, 8-HOUR Average Wear Time, 6/1-patch pouches/box.  Dosage: 120mA/min.",
      "product_quantity": "5,141 primary cartons",
      "reason_for_recall": "The dosage information on the pouch is incorrect; the primary carton label is correct.",
      "recall_initiation_date": "20211110",
      "center_classification_date": "20220105",
      "termination_date": "20230201",
      "report_date": "20220112",
      "code_info": "Lot numbers 1131-1 and 1131-2"
    }
  ]
}