{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Santa Clara",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99176",
      "recalling_firm": "Covidien, LLC",
      "address_1": "3062 Bunker Hill Ln",
      "address_2": "",
      "postal_code": "95054-1105",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - U.S. Nationwide distribution including in the states of AK, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, and WV. The countries of Argentina, Australia, Austria, Belgium, Canada, Colombia, Costa Rica, Denmark, France, Germany, Hong Kong, Ireland, Israel, Italy, Netherlands, New Zealand, Northern Ireland, Norway, Portugal, South Korea, Spain, Sweden, Switzerland, United Kingdom.",
      "recall_number": "Z-2950-2026",
      "product_description": "EndoFLIP System that includes:  ENDOFLIP 1 SYSTEM EF-100  05391530810050  10884521809307  REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1  10884521808096  05391530810166  DL ENDOFLIP 1  10884521786684  Endoscopic measuring system, including catheter components.",
      "product_quantity": "327",
      "reason_for_recall": "The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.",
      "recall_initiation_date": "20260513",
      "center_classification_date": "20260814",
      "report_date": "20260826",
      "code_info": "ENDOFLIP 1 SYSTEM EF-100  05391530810050  10884521809307  REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1  10884521808096  05391530810166  DL ENDOFLIP 1  10884521786684  Catheters used after January 1, 2026.",
      "more_code_info": ""
    }
  ]
}