{
  "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-0498-2013",
      "product_description": "Reusable, non-sterile, self-adhering electrodes for use with TENS/NMES, .  Made in the U.S.A.  Cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.",
      "product_quantity": "2,014 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 202028 and 202722"
    }
  ]
}