{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "105688",
      "product_res_number": "Z-0519-2012",
      "event_date_initiated": "2011-07-26",
      "event_date_posted": "2012-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2016-06-10",
      "res_event_number": "60518",
      "product_code": "FQO",
      "product_description": "Smith & Nephew, SPIDER2 Limb Positioner, including accessories Battery, foot pedal and charger\nCatalog Number: 72203299.\n\nTable, Operating-room, Pneumatic.",
      "code_info": "Serial Numbers: VAL07, VAL08,VAL11,VAL15, VAL16, VAL19, VAL20, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 58, 59, 60, 61, 62, 63, 66, 71, 73, 76, 77, 79, 80, 81, 82, 88, 90, 92, 93, 94, 95, 97, 98, 99, 100, 101, 102, 103, 104, 106, 107, 110",
      "firm_fei_number": "3003604053",
      "recalling_firm": "Smith & Nephew, Inc. Endoscopy Division",
      "address_1": "150 Minuteman Drive",
      "city": "Andover",
      "state": "MA",
      "postal_code": "01810-1031",
      "additional_info_contact": "Same\n978-749-1073",
      "reason_for_recall": "SPIDER2 may unlock (loss of traction) resulting in\npotential movement of the patient when the device is within close proximity to an RF source. Loss\nof traction can potentially result in the unintended repositioning of the extremity and  potential for tissue or cartilage damage",
      "root_cause_description": "Device Design",
      "action": "Smith & Nephew Advanced Surgical Devices Division sent an \"URGENT- PRODUCT RECALL NOTIFICATION-URGENT\" letter dated July 26, 2011 to all affected customers.  The letter described the product, problem, and the actions to be taken by the customers.  Customers were instructed to complete and return a form via fax at 405-917-8650.  Contact the firm at 405-917-8556 for questions regarding this recall.",
      "product_quantity": "52 units",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Canada and France.",
      "openfda": {
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        "device_name": "Table, Operating-Room, Ac-Powered",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4960",
        "device_class": "1"
      }
    }
  ]
}