{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97146",
      "recalling_firm": "LTS Therapy Systems, LLC",
      "address_1": "1685 Marthaler Ln",
      "address_2": "",
      "postal_code": "55118-3517",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of Indiana, Tennessee, New York, Minnesota, New Jersey, Ohio, Kentucky, Illinois, and South Dakota.",
      "recall_number": "Z-2197-2025",
      "product_description": "IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080;   The IontoPatch is an Iontophoresis transdermal patch.",
      "product_quantity": "63936 units",
      "reason_for_recall": "The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.",
      "recall_initiation_date": "20250522",
      "center_classification_date": "20250729",
      "report_date": "20250806",
      "code_info": "Lot Code: UDI-DI: (01) 10815611020012 UDI-PI:  (10) 4303 Lot numbers: 4303-1, 4303-2, 4303-3",
      "more_code_info": ""
    }
  ]
}