{
  "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": "Horsham",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76156",
      "recalling_firm": "Flower Orthopedics Corporation",
      "address_1": "100 Witmer Rd Ste 280",
      "address_2": "N/A",
      "postal_code": "19044-2647",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed throughout the United States",
      "recall_number": "Z-1113-2017",
      "product_description": "Cannulated Drill bit 2.0mm and 2.6 mm; Used in conjunction with the Flower Bone Screw Set.",
      "product_quantity": "N/A",
      "reason_for_recall": "The product is being recalled due to incidence and reports of the product breaking during surgery.",
      "recall_initiation_date": "20161222",
      "center_classification_date": "20170128",
      "termination_date": "20171127",
      "report_date": "20170208",
      "code_info": "Device Listing: D267957",
      "more_code_info": ""
    }
  ]
}