{
  "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": "2026-05-06",
    "results": {
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      "city": "Co. Cork",
      "state": "",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98707",
      "recalling_firm": "DEPUY (IRELAND)",
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      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of MN, NC, TX.",
      "recall_number": "Z-1988-2026",
      "product_description": "Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.",
      "product_quantity": "3 units",
      "reason_for_recall": "The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.",
      "recall_initiation_date": "20260403",
      "center_classification_date": "20260429",
      "report_date": "20260506",
      "code_info": "Part Number: 150450108. UDI-DI: 10603295543022. Lot Number: AF1006441. Expiration Date: 12/31/2035.",
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}