{
  "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": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68243",
      "recalling_firm": "Covidien LLC",
      "address_1": "15 Hampshire Street",
      "address_2": "",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of NJ, CA, TX, IL, MO, PA, OH, IN, MI, MN, FL, IN, DC, PA, VA, MS, ME, NV, AR, KY, NY, KS, SC",
      "recall_number": "Z-1997-2014",
      "product_description": "Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090    Product Usage:  The device is intended to provide padding under the patient, and help maintain the position of an anesthetized patient during surgery.",
      "product_quantity": "264 devices",
      "reason_for_recall": "Straps may separate from the foam pad.",
      "recall_initiation_date": "20140508",
      "center_classification_date": "20140706",
      "termination_date": "20150904",
      "report_date": "20140716",
      "code_info": "14085, 14086, 14092, 14095, 14101, 14106    *The original recall submission listed 14084 and 14094, these were reported by Covidien in error on the original submission.",
      "more_code_info": ""
    }
  ]
}