{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Allendale",
      "address_1": "2 Pearl Ct",
      "reason_for_recall": "The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.",
      "address_2": "",
      "product_quantity": "5",
      "code_info": "Lot Number 7HX",
      "center_classification_date": "20181009",
      "distribution_pattern": "US Nationwide in the states:  CA, FL, GA, MI, MN, NJ, NM, and OR",
      "state": "NJ",
      "product_description": "AVS Aria Cage, Catalog Number 48753212    Product Usage:  The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral body fusion devices indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2 to S1 . The AVS¿ ARIA TM PEEK Spacers are intended to be used with supplemental fixation systems that have been cleared for use in the lumbosacral spine.",
      "report_date": "20181017",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Spine",
      "recall_number": "Z-0092-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80971",
      "termination_date": "20190523",
      "more_code_info": "",
      "recall_initiation_date": "20180813",
      "postal_code": "07401-1611",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}