{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Franklin",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88395",
      "recalling_firm": "BioMimetic Therapeutics, LLC",
      "address_1": "389 Nichol Mill Ln # A",
      "address_2": "N/A",
      "postal_code": "37067-4882",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AK, CA, CO, FL, GA, IA, ID, IL, IN, MA, MI, MN, NC, NJ, NM, NY, OH, OR, PA, TX, UT, VA, WA, and WI.",
      "recall_number": "Z-2335-2021",
      "product_description": "AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343",
      "product_quantity": "499 units",
      "reason_for_recall": "The kit contains the wrong vial tray in the package.",
      "recall_initiation_date": "20210723",
      "center_classification_date": "20210823",
      "termination_date": "20240904",
      "report_date": "20210901",
      "code_info": "Model Number K30003010, Lot 1706343"
    }
  ]
}