{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "112953",
      "product_res_number": "Z-0006-2013",
      "event_date_initiated": "2011-11-14",
      "event_date_posted": "2012-10-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-07-02",
      "res_event_number": "63196",
      "product_code": "FGO",
      "k_numbers": [
        "K962676"
      ],
      "product_description": "Endoscopic retrieval device.\n\nThe disposable Raptor grasping device in intended to retrieve foreign bodies or resected tissue specimens in endoscopic procedures of the upper and lower gastrointestinal tract or biliary tract.",
      "code_info": "Model #00711177; S/N: 52979, 52981, 52982, 53643, 53644, 53891, 53892, 54238",
      "firm_fei_number": "1000122656",
      "recalling_firm": "US Endoscopy Group Inc",
      "address_1": "5976 Heisley Rd",
      "city": "Mentor",
      "state": "OH",
      "postal_code": "44060-1873",
      "additional_info_contact": "Craig L. Moore\n440-639-4494 Ext. 378",
      "reason_for_recall": "When the outer catheter is either coiled or in a contorted configuration outside of the endoscope and the patient, and excessive force is applied to the handle, the jaws may become inoperable and may become stuck in the open condition.",
      "root_cause_description": "Device Design",
      "action": "US Endoscopy initiated a Voluntary Product Recall letter initiated November 11, 2011. The letter identified the product the problem and the action needed to be taken by the customer.\n\nUS Endoscopy will provide a free replacement or grant your facility a credit toward a future purchase for every device that is returned to US Endoscopy or verified as having been used or destroyed.\n\nFor further questions please call 440-639-4494 ext. 378.",
      "product_quantity": "1153",
      "distribution_pattern": "Worldwide Distribution -- USA (nationwide) including the states of  AL, AR, AZ, CA, FL, GA, HI, IA, IL, KY, LA, MD, ME, MI, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, and WI; and to the following countries: Argentina, Australia, Austria, Bahrain, Belgium, Brazil, Caribbean, Chile, Columbia, Croatia, Czech Republic, Denmark, Ecuador, El Salvador, Estonia, Finland, France, Germany, Great Britain, Greece, India, Ireland, Israel, Italy, Jordan, Lithuania, Malta, Mexico, Netherlands, New Zealand, Norway, Panama, Poland, Portugal, Romania, Saudi Arabia, Slovenia, South Africa, Spain, Switzerland, Turkey, and United Arab Emirates.",
      "openfda": {
        "device_name": "Dislodger, Stone, Flexible",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.4680",
        "device_class": "2",
        "k_number": [
          "K914110",
          "K895080",
          "K891252",
          "K896322",
          "K970121",
          "K962676",
          "K893522",
          "K922542",
          "K921295",
          "K933261",
          "K891253",
          "K951309",
          "K885168",
          "K771302",
          "K934598",
          "K001563",
          "K914111",
          "K914112",
          "K963750"
        ],
        "registration_number": [
          "2936485",
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        "fei_number": [
          "2936485",
          "3005747797",
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}