{
  "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": "Clarkston",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80234",
      "recalling_firm": "Safe N Simple, LLC",
      "address_1": "5827 Terex",
      "address_2": "N/A",
      "postal_code": "48346-1717",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributors in two states: AL and OH.",
      "recall_number": "Z-2229-2018",
      "product_description": "DermaPro Waterproof Silicone Tape, SNS57232",
      "product_quantity": "318 rolls",
      "reason_for_recall": "The recalling firm received a customer complaint stating the tape was difficult to peel off the roll and had poor adhesion.",
      "recall_initiation_date": "20171214",
      "center_classification_date": "20180614",
      "termination_date": "20190404",
      "report_date": "20180620",
      "code_info": "20170716."
    }
  ]
}