{
  "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": 1
    }
  },
  "results": [
    {
      "cfres_id": "104517",
      "product_res_number": "Z-0435-2012",
      "event_date_initiated": "2011-09-21",
      "event_date_posted": "2012-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-09-27",
      "res_event_number": "60138",
      "product_code": "NRA",
      "product_description": "\"***BUECHEL-PAPPAS Conforming Bearing***UHMWPE***SIZE***CAT**STERILE***ENDOTEC***Endotec, Inc. 300 Sunport Lane, Suite 500 Orlando, FL 32809 USA***\"\n\nSIZE 1 x 10mm CAT 04-33-0041;     \nSIZE 2 x 10mm CAT 04-33-0042;     \nSIZE 3 x 10mm CAT 04-33-0043;     \nSIZE 4 x 10mm CAT 04-33-0044;     \nSIZE 5 x 10mm CAT 04-33-0045;     \nSIZE 6 x 10mm CAT 04-33-0046.  \n\nTricompartmental Knee Replacement",
      "code_info": "K04330041A1NN467 K04330041A2NN741 K04330042A1NN467 K04330042A2NN467 K04330042A3NN741 K04330043A1NN467 K04330043A2NN467 K04330043A3NN741 K04330044A1NN467 K04330044A2NN741 K04330045A1NN742 K04330046A1NN742",
      "firm_fei_number": "3004553437",
      "recalling_firm": "Endotec, Inc.",
      "address_1": "300 Sunport Ln Ste 500 300 Sunport Ln",
      "address_2": "Ste 500",
      "city": "Orlando",
      "state": "FL",
      "postal_code": "32809-8123",
      "additional_info_contact": "Faranak Gomarooni\n800-323-9890",
      "reason_for_recall": "On 09/21/2011 Endotec, Orlando, FL initiated a recall for the Beuchel-Pappas Mobile Bearing Knee System (BP Knee).  The BP Mobile Bearing Knee System consists of unapproved mobile (rotating) bearing tibial and patellar components.",
      "root_cause_description": "PMA",
      "action": "Endotec sent an \"URGENT: MEDICAL DEVICE RECALL\" letter dated September 21, 2011 to all affected customers.  The letter described the product, problem, and actions to be taken by the customers.  The letter instructs customers to examine and quarantine product subject to the recall. Additionally, a Response Form was included with the letter for customers to complete and return to the firm.  Call 862-703-6730 for questions regarding this recall.",
      "product_quantity": "146",
      "distribution_pattern": "USA (nationwide) including the states of AZ, CA, CT, FL, NE, NJ, OH, and OK.",
      "openfda": {
        "pma_number": [
          "P010014",
          "P910016"
        ],
        "registration_number": [
          "3007963827",
          "1818910",
          "3006801265",
          "3012392319",
          "1450662",
          "3002806535",
          "3013055499",
          "3006946279",
          "1721676",
          "3004748528",
          "1822565",
          "3007923096",
          "1825034",
          "3014315560",
          "3002807310"
        ],
        "fei_number": [
          "3007963827",
          "1818910",
          "3006801265",
          "3012392319",
          "1450662",
          "3002806535",
          "3013055499",
          "3006946279",
          "1721676",
          "3004748528",
          "1825034",
          "3007923096",
          "1000220733",
          "3014315560",
          "3002807310"
        ],
        "device_name": "Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}