{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Valencia",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84983",
      "recalling_firm": "Boston Scientific Neuromodulation Corporation",
      "address_1": "25155 Rye Canyon Loop",
      "address_2": "N/A",
      "postal_code": "91355-5004",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed OUS only. to 14 countries.",
      "recall_number": "Z-2120-2020",
      "product_description": "Thirty-five (35) cm 8 Contact Extension Kit, part number M365SC3138350.  Package Contents:  Lead Extension Kit  (1) Lead Extension  (1) Hex Wrench  (1) Tunneling Tool Assembly  (1) Device Registration Form/Temporary Patient Identification Card  (1) Manual  Product Usage: Contact extension kits are part of a spinal cord stimulation system for prescription use only as an aid in the management of chronic intractable pain of the trunk and/or limbs. They are designed to connect the percutaneous leads to the Implantable Pulse Generator (IPG) for spinal cord stimulation.",
      "product_quantity": "19 units",
      "reason_for_recall": "The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to the  \"use by date\" displayed on the label which is later than the correct \"use by date\". No adverse health consequence is expected to occur from this issue.",
      "recall_initiation_date": "20190424",
      "center_classification_date": "20200526",
      "termination_date": "20220118",
      "report_date": "20200603",
      "code_info": "Part number M365SC3138350; serial numbers 1041034, 1055172, 3000549, 1041380, 1056806, 3000564, 1053375, 1058008, 3001907, 1053695, 1058015, 3007457, 1053700, 1058017, 3008119, 1054299, 1062660, 1054304, and 1064590."
    }
  ]
}