{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Westminster",
      "state": "CO",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90015",
      "recalling_firm": "Cerapedics, Inc.",
      "address_1": "11025 Dover St Unit 1600",
      "address_2": "N/A",
      "postal_code": "80021-5574",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S. Nationwide distribution in the states of  AL, AZ, CA, CT, DC, DE, ID, IN, KS, KY, MD, MI, MN, MO, NC, NV, NY, OH, PA, TX, VA, and WA.",
      "recall_number": "Z-1056-2022",
      "product_description": "putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY",
      "product_quantity": "572 units",
      "reason_for_recall": "Patient chart label contains incorrect Part Number and volume amount.",
      "recall_initiation_date": "20220414",
      "center_classification_date": "20220510",
      "termination_date": "20241223",
      "report_date": "20220518",
      "code_info": "Model/Catalog Number: 700-010 UDI Code: (01)00850001680004(17)240531(10)21C0991 Lot Number: 21C0991"
    }
  ]
}