{
  "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": [
    {
      "country": "United States",
      "city": "Elkton",
      "address_1": "950 Elkton Blvd",
      "reason_for_recall": "Medical devices were incorrectly labeled with extended expiration dates.",
      "address_2": "",
      "product_quantity": "20 units",
      "code_info": "Lot MM27",
      "center_classification_date": "20130627",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "MD",
      "product_description": "Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve.    Acts as a conduit to facilitate the introduction of interventional and diagnostic devices into the human vasculature.",
      "report_date": "20130703",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Terumo Medical Corporation",
      "recall_number": "Z-1611-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65397",
      "termination_date": "20131030",
      "more_code_info": "",
      "recall_initiation_date": "20130530",
      "postal_code": "21921-5322",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}