{
  "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": [
    {
      "country": "United States",
      "city": "Morrisville",
      "address_1": "1380 S Pennsylvania Ave",
      "reason_for_recall": "Small Bone Innovations (SBi) is recalling all lots of 3.0/4.0mm AutoFIX\"  Cannulated Compression Screw System Sets, Implants, and Instruments to update the IFU.",
      "address_2": "",
      "product_quantity": "506",
      "code_info": "All lots",
      "center_classification_date": "20140730",
      "distribution_pattern": "Nationwide Distribution including TN, OK, AZ, PA, TX, MO, NY, NC, CA, FL, WA, AL, IN, NH, SD, and OH.",
      "state": "PA",
      "product_description": "Small Bone Innovations 3.0/4.0mm AutoFIX\"  Cannulated Compression Screw System Sets, Implants, and Instruments      Indications for Use: AutoFIX\" cannu lated screws are indicated for the treatment of fractures, non-unions, pseudoarthrosis and degenerative changes as well as corrective osteotom ies geared towards a functionally stable osteosynthesis in small bones.",
      "report_date": "20140806",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Small Bone Innovations",
      "recall_number": "Z-2127-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68445",
      "termination_date": "20141008",
      "more_code_info": "",
      "recall_initiation_date": "20140519",
      "postal_code": "19067",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}