{
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    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-08",
    "results": {
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      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97720",
      "recalling_firm": "Prismatik Dentalcraft, Inc.",
      "address_1": "2144 Michelson Dr",
      "address_2": "N/A",
      "postal_code": "92612-1304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: California, Colorado, Connecticut, Florida, Georgia, Hawaii, Kentucky, Maryland, Massachusetts, Michigan, New Hampshire, New Jersey, New York, Pennsylvania, South Carolina, Tennessee, Virginia, Washington.",
      "recall_number": "Z-0417-2026",
      "product_description": "Brand Name: Inclusive  Product Name: Inclusive Titanium Screw compatible with: Biomet 3i\" Certain 3.4/4.1/5.0/6.0 mm  Model/Catalog Number: 70-1047-COM0117",
      "product_quantity": "208 units",
      "reason_for_recall": "Incorrect titanium screw, packaged with dental implant.",
      "recall_initiation_date": "20250930",
      "center_classification_date": "20251103",
      "report_date": "20251112",
      "code_info": "Lot Code: Product Catalog Number (SKU#): 70-1047-COM0117 UDI: +D745701047COM01170/$$80176270484/16D20250722E Lot Number: 6270484, 6271089",
      "more_code_info": ""
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