{
  "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": "2026-04-15",
    "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": "72418",
      "recalling_firm": "Teleflex Medical",
      "address_1": "2917 Weck Dr",
      "address_2": "N/A",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including the states of  AK, AZ, AR, CA, CT, FL, GA, ID, IL, IN, IA, KY, LA, ME, MD, MA, MI, MN, MO, MT, NE, NJ, NY, NC, OH, OK, PA, TN, TX, VA, VT, and WI.",
      "recall_number": "Z-0277-2016",
      "product_description": "Taut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93.  To provide an access port into the peritoneal cavity.",
      "product_quantity": "2050 ea.",
      "reason_for_recall": "The defective component can cause gas leakage through the device.  This can result in loss of pneumoperitoneum, potentially necessitating removal  of the defective device and insertion of another device.",
      "recall_initiation_date": "20151014",
      "center_classification_date": "20151116",
      "termination_date": "20171211",
      "report_date": "20151125",
      "code_info": "Lot Numbers - 73A1500175, 73A1500306, 73B1500116, 73B1500418"
    }
  ]
}