{
  "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": [
    {
      "status": "Terminated",
      "city": "Shelton",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65968",
      "recalling_firm": "Spine Wave, Inc.",
      "address_1": "3 Enterprise Dr Ste 302",
      "address_2": "N/A",
      "postal_code": "06484-4694",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed in the states of FL and OR.",
      "recall_number": "Z-2187-2013",
      "product_description": "StaXx¿ IB Convex Expandable Implant (25 x 12 x 9 mm), Intervertebral Fusion Device, Lumbar; Catalog Number 11 -1902.    Indicated for intervertebral body fusion procedures in skeletally mature patients.",
      "product_quantity": "17 units",
      "reason_for_recall": "A component Superior endplate manufactured from a different polymer than specified",
      "recall_initiation_date": "20130514",
      "center_classification_date": "20130911",
      "termination_date": "20140210",
      "report_date": "20130918",
      "code_info": "Lot Numbers: 272L08 and 272L09",
      "more_code_info": ""
    }
  ]
}