{
  "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": {
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  "results": [
    {
      "status": "Completed",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91947",
      "recalling_firm": "Medacta Usa Inc",
      "address_1": "3973 Delp St",
      "address_2": "N/A",
      "postal_code": "38118-6110",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US:  ID, TX, GA, VA, AZ",
      "recall_number": "Z-1403-2023",
      "product_description": "MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device",
      "product_quantity": "34 units",
      "reason_for_recall": "There is a potential for breakage of the small screw used to affix the anti-backout plate.",
      "recall_initiation_date": "20230308",
      "center_classification_date": "20230419",
      "report_date": "20230426",
      "code_info": "UDI/DI 07630345732316, All Lot Numbers"
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}