{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Wabasha",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "61209",
      "recalling_firm": "Covidien LLC dba Uni-Patch",
      "address_1": "1313 Grant Blvd W",
      "address_2": "N/A",
      "postal_code": "55981-1058",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide Distribution including CA, IL, MA, MN, and SD.",
      "recall_number": "Z-0499-2013",
      "product_description": "Reusable, Self-Adhering TENS/NMES/FES electrodes Single Patient Use Only.     An electrocardiograph electrode is the electrical conductor which is applied to the surface of the body to transmit the electrical signal at the body surface to a processor that produces an electrocardiogram or vectorcardiogram.",
      "product_quantity": "3594 pouches",
      "reason_for_recall": "Covidien is conducting a voluntary recall regarding specific lots of TENS electrodes because it was determined that during the manufacturing process the surface of the wires in these lots may have been exposed to an employee who had a minor cut.",
      "recall_initiation_date": "20120209",
      "center_classification_date": "20121210",
      "termination_date": "20130103",
      "report_date": "20121219",
      "code_info": "Lots 202404, 202506, 203431,"
    }
  ]
}