{
  "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": [
    {
      "country": "United States",
      "city": "Marietta",
      "address_1": "1755 W Oak Pkwy",
      "reason_for_recall": "Absent tantalum market pin.",
      "address_2": "",
      "product_quantity": "6 devices",
      "code_info": "Part Number 08-170-1010 - Lot Number 134926; Part Number 08-170-1011 - Lot Number 134927;  Part Number 08-170-1006 - Lot Number 134929; Part Number 08-170-1008 - Lot Number 134931",
      "center_classification_date": "20170109",
      "distribution_pattern": "US Distribution to GA only.",
      "state": "GA",
      "product_description": "Ceres-C Standalone Cervical Interbody    The product is a stand-alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying radicular symptoms at the one level from C2-T1.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Amendia, Inc",
      "recall_number": "Z-0966-2017",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "75857",
      "termination_date": "20170228",
      "more_code_info": "",
      "recall_initiation_date": "20161122",
      "postal_code": "30062-2260",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}