{
  "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,
      "total": 75
    }
  },
  "results": [
    {
      "cfres_id": "35052",
      "product_res_number": "Z-0009-05",
      "event_date_initiated": "2004-09-17",
      "event_date_posted": "2004-10-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-08-05",
      "res_event_number": "30036",
      "product_code": "KXN",
      "k_numbers": [
        "K923636"
      ],
      "product_description": "Applied Blunt Tip Trocar\n\nModels C0717 and C0718",
      "code_info": "Trocars are assembled into procedure kits. Trocars have thier own serial number but the kit lots are relevant and include:  45036301001 to 45036301007 containing 1 each of lot 126803 = 71 each; 45208001001 to 452084001008 containing 1 each of lot 127322=8 each; 452451005001 to 452451005003 containing 1 each of lot 127322=3 each; 453029001001 to 453029001017 containing 1 each of lot 127322 = 17 each; 453715004002 containing 1 each of lot 126803 = 1 each; 454116005001 to 454116005002 containing 1 each of lot 127322 = 2; 454608003001 to 454608003006 containing 1 each of lot 172528 = 6 each.",
      "firm_fei_number": "2027111",
      "recalling_firm": "Applied Medical Resources Corp",
      "address_1": "22872 Avenida Empresa # 3 # 3 avenida empresa",
      "city": "Rancho Santa Margarita",
      "state": "CA",
      "postal_code": "92688-2650",
      "additional_info_contact": "mary Jo Stegwell\n949-713-8000",
      "reason_for_recall": "Inadequate trocar tip assembly that might yeild parts to patients.",
      "root_cause_description": "Other",
      "action": "Initiated recall by letter on 9/16/2004 via Fedex/UPS. Follow-up to nonresponders in 30 days.",
      "product_quantity": "1025",
      "distribution_pattern": "Nationwide. Ireland.",
      "openfda": {
        "k_number": [
          "K760968",
          "K770245"
        ],
        "device_name": "Monitor, Cardiac, Fetal",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.2600",
        "device_class": "2"
      }
    }
  ]
}