{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Carlsbad",
      "address_1": "3115 Melrose Dr",
      "reason_for_recall": "Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.",
      "address_2": "Suite 200",
      "product_quantity": "68 units total",
      "code_info": "Lot Number: 080589",
      "center_classification_date": "20130507",
      "distribution_pattern": "Distributed in OH and PA.",
      "state": "CA",
      "product_description": "Mercury Spinal System DIA 5.5 x 100mm Lordosed Rod,  Part Number: 60100-100.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.",
      "report_date": "20130515",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Spinal Elements, Inc",
      "recall_number": "Z-1253-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "53487",
      "termination_date": "20130507",
      "recall_initiation_date": "20090417",
      "postal_code": "92010-6690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}