{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Rillieux La Pape",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92738",
      "recalling_firm": "Medicrea International",
      "address_1": "Vancia",
      "address_2": "Vancia",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide",
      "recall_number": "Z-2454-2023",
      "product_description": "IMPIX ALIF S/A, REF number B15241415;   intervertebral fusion device - lumbar",
      "product_quantity": "5 units",
      "reason_for_recall": "There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.",
      "recall_initiation_date": "20230712",
      "center_classification_date": "20230824",
      "report_date": "20230830",
      "code_info": "GTIN 03613720264439, Lot Numbers:  18I0824, 19L0046"
    }
  ]
}