{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Burke",
      "address_1": "6337 Falling Brook Dr",
      "reason_for_recall": "The implant size is incorrectly etched on the implant. The size listed on the box is correct.",
      "address_2": "",
      "product_quantity": "6",
      "code_info": "Lot 1599, Expiration date: 10/03/2018",
      "center_classification_date": "20180410",
      "distribution_pattern": "The devices were distributed in California.",
      "state": "VA",
      "product_description": "Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 W x 25 L    Product Usage:  The Spinal Jaxx interbody fusion device is indicated for spinal fusion for patients with degenerative disc disease (DDD) at one or two contiguous levels of the lumbosacral spine (L2-S1). DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. Patients may also have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The indicated patient population is skeletally mature patients who have had six (6) months of non-operative treatment. The Spinal Jaxx interbody fusion device must be used with autogenous bone graft material and with supplemental fixation.",
      "report_date": "20180418",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Neuropro Spinal Jaxx",
      "recall_number": "Z-1350-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79559",
      "termination_date": "20180713",
      "more_code_info": "",
      "recall_initiation_date": "20180118",
      "postal_code": "22015-4031",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}