{
  "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": "Research Triangle Park",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67972",
      "recalling_firm": "Teleflex Medical",
      "address_1": "2917 Weck Dr.",
      "address_2": "N/A",
      "postal_code": "27709",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution -- USA, including the state of MA, and the country of Germany",
      "recall_number": "Z-1509-2014",
      "product_description": "Monodek Violet Synthetic Absorbable Surgical Sutures, MF 0 TC43/HR26 48",
      "product_quantity": "3,072 ea.",
      "reason_for_recall": "Product does not meet minimum knot tensile strength requirements.",
      "recall_initiation_date": "20140311",
      "center_classification_date": "20140424",
      "termination_date": "20170925",
      "report_date": "20140430",
      "code_info": "Product Code: 833-137, Batch: 02H1103434, 02H1200349, and 02K1201354.",
      "more_code_info": ""
    }
  ]
}