{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83250",
      "recalling_firm": "Teleflex Medical",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "N/A",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution to CA, FL, IL, NC, NJ, OH, OK, TX.",
      "recall_number": "Z-2086-2019",
      "product_description": "Rusch EasyCath Kit",
      "product_quantity": "3,700 devices",
      "reason_for_recall": "Potential for product not to be sterile.",
      "recall_initiation_date": "20190701",
      "center_classification_date": "20190726",
      "termination_date": "20211104",
      "report_date": "20190807",
      "code_info": "Catalog Number ECK120, Lot Number 74C1900304, Expiration Date 03/01/2022.  Catalog Number ECK125, Lot Number 74B1901676, Expiration Date 06/01/2022."
    }
  ]
}