{
  "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": "Research Triangle Park",
      "address_1": "2917 Weck Dr",
      "reason_for_recall": "Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).",
      "address_2": "",
      "product_quantity": "8",
      "code_info": "Lot K3",
      "center_classification_date": "20160316",
      "distribution_pattern": "US Distribution to the state of : UT",
      "state": "NC",
      "product_description": "Pilling Modular Verres Body/Obturator, Product Code 140880",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teleflex Medical",
      "recall_number": "Z-1178-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73267",
      "termination_date": "20170414",
      "more_code_info": "",
      "recall_initiation_date": "20150108",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}