{
  "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": "2026-07-08",
    "results": {
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      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94215",
      "recalling_firm": "Howmedica Osteonics Corp.",
      "address_1": "325 Corporate Dr",
      "address_2": "N/A",
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      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
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      "recall_number": "Z-1622-2024",
      "product_description": "TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation  Catalog Number: 702-11-48D",
      "product_quantity": "45 units",
      "reason_for_recall": "The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell",
      "recall_initiation_date": "20240227",
      "center_classification_date": "20240425",
      "report_date": "20240501",
      "code_info": "UDI-DI: (01)07613327380903(17)290313(10) Lot Number:  14875651 15005253 16044255",
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}