{
  "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-2122-2020",
      "product_description": "The LinearTM 3-4 70 cm 8 Contact Lead Kit, part number M365SC2352700 is  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.     Package Contents  Percutaneous Permanent Lead Kits  (1) Percutaneous Lead with pre-loaded Curved Stylet  (1) Stylet Ring with a Curved and a Straight Stylet  (4) Suture Sleeves  (1) Insertion Needle with Stylet  (1) Lead Blank  (1) Steering Cap  (1) OR Cable Assembly  (2) Lead Position Labelsleft and right (non-sterile)  (1) Device Registration Form/Temporary Patient Identification Card  (1) Manual",
      "product_quantity": "1 unit",
      "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 M365SC2352700; serial number 1042757."
    }
  ]
}