{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95978",
      "recalling_firm": "IsoTis OrthoBiologics, Inc.",
      "address_1": "2 Goodyear Ste A",
      "address_2": "",
      "postal_code": "92618-2052",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, MD. MN, MS, NC, NV, OH, OK, TX.",
      "recall_number": "Z-0919-2025",
      "product_description": "OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01.",
      "product_quantity": "145",
      "reason_for_recall": "Hydration issue resulting in the product being less cohesive and moldable than intended due to an issue with the polymer.",
      "recall_initiation_date": "20241127",
      "center_classification_date": "20250115",
      "report_date": "20250122",
      "code_info": "OsteoCove Putty, REF 56920013, UDI-DI: 10889981309022, Lot Numbers: 180054, Exp. 2025-08-28; 180054R18, Exp. 2025-08-28; 179604R18, Exp. 2024-12-28; 180484, Exp. 2026-02-28; 180370, Exp. 2026-01-28; 180299, Exp. 2025-11-28; 180075, Exp. 2025-08-28; and   Cove Putty, REF 02-9200-013, UDI-DI: 10889981308933, Lot Number: 180075R18, Exp. 2025-08-28.",
      "more_code_info": ""
    }
  ]
}