{
  "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": "Marietta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75855",
      "recalling_firm": "Amendia, Inc",
      "address_1": "1755 W Oak Pkwy",
      "address_2": "N/A",
      "postal_code": "30062-2260",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : GA. MI, OK, SC, TX, VA",
      "recall_number": "Z-0827-2017",
      "product_description": "Zeus-P Lumbar Interbody Device",
      "product_quantity": "25 units",
      "reason_for_recall": "Labeling error where three boxes in inventory had conflicting patient and primary labels. Evaluation indicated that the primary label and patient label did not match.  The primary label matched the label on the inner pouch, but the patient label was incorrect.",
      "recall_initiation_date": "20161122",
      "center_classification_date": "20161220",
      "termination_date": "20170605",
      "report_date": "20161228",
      "code_info": "Part Number 1-110926B - Lot Number 128945 and Part Number 1-120922B - Lot Number 128946"
    }
  ]
}