{
  "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": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75301",
      "recalling_firm": "Medtronic",
      "address_1": "60 Middletown Ave",
      "address_2": "N/A",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (Nationwide)  Foreign:  Austria  Belgium  Bulgaria  Brazil  Chile  Cyprus  Denmark  Egypt  Finland  France  France  Germany  Greece  Hungary  Iran  Ireland  Israel  Italy  Japan  Kenya  Kuwait  Latvia  Luxembourg  Mexico  Namibia  Netherlands  Nigeria  Norway  Poland  Portugal  Romania  Saudi Arabia  Serbia  Slovakia  South Africa  Spain  Sweden  Switzerland  Turkey  United Arab Emirates  United Kingdom",
      "recall_number": "Z-0890-2017",
      "product_description": "Best Practices kits containing certain production lots of Clearify Visualization System  Item  Code: 21-345  Intended to be used prior to and during endoscopic and laparoscopic procedures to prevent fogging of the scope as well as clean the scope lens",
      "product_quantity": "230 systems",
      "reason_for_recall": "Product sterility is compromised due to breach of the sterile barrier",
      "recall_initiation_date": "20161004",
      "center_classification_date": "20161222",
      "termination_date": "20180808",
      "report_date": "20161228",
      "code_info": "Kit Parent Codes:  00Z2224  00Z2232  00Z2298  00Z2363   00Z2364   00Z2365  00Z2366   00Z2421   00Z2425  00Z2430   00Z2431   00Z2460  00Z2493    00Z2534    00Z2535    000Z2544   00Z5000B   00Z5001B   GYNKIT2"
    }
  ]
}