{
  "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": "550 units",
      "code_info": "Lot MP08",
      "center_classification_date": "20130627",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "MD",
      "product_description": "Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060.    Used to facilitate placing a catheter through the skin into a vein or artery.",
      "report_date": "20130703",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Terumo Medical Corporation",
      "recall_number": "Z-1612-2013",
      "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"
    }
  ]
}