{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "50019",
      "product_res_number": "Z-0414-2007",
      "event_date_initiated": "2006-10-19",
      "event_date_posted": "2007-02-08",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-10-31",
      "res_event_number": "37162",
      "product_code": "NLM",
      "k_numbers": [
        "K043594"
      ],
      "product_description": "AutoSuture Bladed Trocar, equipped with safety shield. Model number 179094. Available with smooth or threaded sleeve in sizes 5-15mm inner diameter and 70-100mm length.",
      "code_info": "94724\t95261\t104057 94853\t95272\t104217 94893\t100062\t104335 94894\t102389\t104337 94897\t102394\t104343 94953\t102681\t104584 94957\t102851\t105517 94962\t103100\t 94964\t103103\t 95024\t103200\t 95026\t103288\t 95029\t103293\t 95069\t103297\t 95135\t103566\t 95259\t103570",
      "firm_fei_number": "1000132435",
      "recalling_firm": "Ascent Healthcare Solutions, Inc.",
      "address_1": "5307 Great Oak Dr",
      "city": "Lakeland",
      "state": "FL",
      "postal_code": "33815",
      "reason_for_recall": "The tip of the trocars may separate before and while in use. In some instances the trocars have been found with exposed blades upon opening the packaging.",
      "root_cause_description": "Process design",
      "action": "The recall was initiated on 10/19/2006 by direct distribution of the recall notice to direct accounts by the firm's sales force. The firm also posted the notification on their web site. All customers were instructed to examine their inventories for the product and to remove and quarantine all affected product. Instructions on returning the product to the firm were also included along with a response form.",
      "product_quantity": "1566",
      "distribution_pattern": "Nationwide",
      "openfda": {
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          "K043592",
          "K063788",
          "K012578",
          "K062497",
          "K053585",
          "K070059",
          "K111002",
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          "K052299",
          "K043253",
          "K133414",
          "K060676",
          "K100080",
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          "K132629",
          "K172093",
          "K201511",
          "K172097",
          "K160740",
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        "device_name": "Laparoscope, General & Plastic Surgery, Reprocessed",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.1500",
        "device_class": "2"
      }
    }
  ]
}