{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "104957",
      "product_res_number": "Z-0437-2012",
      "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 CRUCIATE SACRIFICING BEARING ***MATERIAL UHMWPe***STERILE EO***ENDOTEC***Endotec, Inc. 300 Sunport Lane, Suite 500 Orlando, FL 32809 USA***CAT.NO.***SIZE***\"\n\nSIZE 3-3X2.5 CAT 04-63-2113;     \nSIZE 3-4X2.5 CAT 04-63-2114;     \nSIZE 3-5X2.5 CAT 04-63-2115;     \nSIZE 3-6X2.5 CAT 04-63-2116.  \n\n Tricompartmental Knee Replacement",
      "code_info": "LOT #'S: 04632113ANN172 04632114BNN249 04632114BNN261 04632115BNN249 04632115BNN261 04632116ANN172",
      "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": "55",
      "distribution_pattern": "USA (nationwide) including the states of AZ, CA, CT, FL, NE, NJ, OH, and OK.",
      "openfda": {
        "pma_number": [
          "P010014",
          "P910016"
        ],
        "registration_number": [
          "3006801265",
          "3013055499",
          "3007963827",
          "3007923096",
          "3002806535",
          "3004748528",
          "3006946279",
          "1825034",
          "3014315560",
          "1450662",
          "3012392319",
          "1818910",
          "3002807310",
          "1822565",
          "1721676"
        ],
        "fei_number": [
          "3006801265",
          "3013055499",
          "3007963827",
          "3007923096",
          "3002806535",
          "3004748528",
          "3006946279",
          "1825034",
          "3014315560",
          "1450662",
          "3012392319",
          "1818910",
          "1000220733",
          "3002807310",
          "1721676"
        ],
        "device_name": "Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}