{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "49022",
      "product_res_number": "Z-0299-2007",
      "event_date_initiated": "2006-09-21",
      "event_date_posted": "2007-01-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-01-25",
      "res_event_number": "36624",
      "product_code": "LGW",
      "pma_numbers": [
        "P030017"
      ],
      "product_description": "Advanced Bionics Precision Linear Leads, part of the Precision Spinal Cord Stimulation System.  Model Numbers: SC-2138-30, SC-2138-50, SC-2138-50T and SC-2138-70.",
      "code_info": "Serial Numbers: 111744, 112122, 112141, 112224, 112233, 114114, 116547, 116553, 117860, 117907, 110490, 100600, 110625, 110809, 113745, 113780, 112055 and 118943",
      "firm_fei_number": "1000220815",
      "recalling_firm": "Advanced Bionics Corporation",
      "address_1": "12740 San Fernando Rd Bldgs. 1 & 3",
      "city": "Sylmar",
      "state": "CA",
      "postal_code": "91342",
      "additional_info_contact": "Kaoru Lee Adair\n661-362-1669",
      "reason_for_recall": "A small number of unimplanted Precision Linear Leads may have been assembled with incorrect electrode material.  At high stimulation levels, the metal may corrode and dissolved metals may enter the patient.",
      "root_cause_description": "Other",
      "action": "In United States, the clinician recall notification letters were distributed by Fed-Ex or U.S. Postal Service certified mail on 09/21/2006. For the other regions, the in-country representatives started providing notification to the clinicians on 09/21/2006.\nThe recall notification letters will instruct physicians to immediately return the unimplanted units.",
      "product_quantity": "18",
      "distribution_pattern": "Worldwide.",
      "openfda": {
        "pma_number": [
          "P130022",
          "P130028",
          "P800040",
          "P030017",
          "P010032",
          "P190002",
          "P210037",
          "P840001"
        ],
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        "fei_number": [
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        ],
        "device_name": "Stimulator, Spinal-Cord, Totally Implanted For Pain Relief",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}