{
  "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": [
    {
      "country": "United States",
      "city": "Research Triangle Park",
      "address_1": "2917 Weck Dr",
      "reason_for_recall": "",
      "address_2": "",
      "product_quantity": "19,043 units  in total",
      "code_info": "Product Code: PE103, Lot numbers: 02B1300991, 02B1402029, 02C1301654, 02E1201155, 02H1302224, 02K1100520, 02K1103125, 02K1200732, 02K1202185, 02L0701465, 02L0701959, 02L1201668, 02L1203112, 02M1201149, 74A1601005 & 74F1400876.74H1601152, 74J1601641, 74K1501590 & 74L1500555.",
      "center_classification_date": "20170522",
      "distribution_pattern": "Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.",
      "state": "NC",
      "product_description": "INFANT 20/BX, Sterile, Single use    Product Usage:  Catheter Connector/Accessory",
      "report_date": "20170531",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teleflex Medical",
      "recall_number": "Z-2130-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77081",
      "termination_date": "20200127",
      "more_code_info": "",
      "recall_initiation_date": "20170421",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}