{
  "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": "104501",
      "product_res_number": "Z-0431-2012",
      "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 0mm CAT 04-33-0001;     \nSIZE 2 x 0mm CAT 04-33-0002;     \nSIZE 3 x 0mm CAT 04-33-0003;     \nSIZE 4 x 0mm CAT 04-33-0004;     \nSIZE 5 x 0mm CAT 04-33-0005;     \nSIZE 6 x 0mm CAT 04-33-0006.  \n\nTricompartmental Knee Replacement",
      "code_info": "04330001Z001NN435 04330001Z005NN436 K04330002A1NN459 K04330002A2NN712 04330003ONN700 04330004NNN462 K04330004B1NN702 04330005Z001NN435 04330005NNN459 K04330005AANN733 04330005AANN736 04330005ABNN751 04330006Z001NN437 04330006H1NN749",
      "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": "730",
      "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"
      }
    }
  ]
}