{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Centennial",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67986",
      "recalling_firm": "AlloSource, Inc.",
      "address_1": "6278 S Troy Cir",
      "address_2": "N/A",
      "postal_code": "80111-6422",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US nationwide, including Michigan and a distributor in Colorado.",
      "recall_number": "Z-1562-2014",
      "product_description": "AlloFuse DBM Putty 5cc, Catalog No. 90038005    AlloFuse is indicated for orthopedic applications as filler for gaps or voids that are not intrinsic to the stability of the bony structure. AlloFuse is indicated to be packed gently into bony gaps in the skeletal system as a bone graft extender.",
      "product_quantity": "29",
      "reason_for_recall": "The donor was hemodiluted.",
      "recall_initiation_date": "20140325",
      "center_classification_date": "20140506",
      "termination_date": "20140811",
      "report_date": "20140514",
      "code_info": "Lot numbers 132095-603, 608, 609, 611-618, 622-629, 631-634, and 636-638. Lot numbers 132095-604, 619, and 621."
    }
  ]
}