{
  "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": "Ongoing",
      "city": "Edison",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93853",
      "recalling_firm": "Musculoskeletal Transplant Foundation, Inc.",
      "address_1": "125 May St Ste 300",
      "address_2": "N/A",
      "postal_code": "08837-3264",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "Product was distributed to Minnesota.",
      "recall_number": "Z-1067-2024",
      "product_description": "AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)",
      "product_quantity": "50",
      "reason_for_recall": "Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.",
      "recall_initiation_date": "20231222",
      "center_classification_date": "20240209",
      "report_date": "20240221",
      "code_info": "UDI-DI: W4184227005T0473  Donor Lots 00322029241137 and 00322039641144"
    }
  ]
}