{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76824",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "130 & 120 Forbes Blvd",
      "address_2": "N/A",
      "postal_code": "02048",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (Nationwide) and Internationally to AU,  CL, DB, DE, ES, FR, GB, NL, SE",
      "recall_number": "Z-1847-2017",
      "product_description": "Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM  Product Number: 72204046  The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone",
      "product_quantity": "N/A",
      "reason_for_recall": "Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming",
      "recall_initiation_date": "20170315",
      "center_classification_date": "20170418",
      "termination_date": "20180710",
      "report_date": "20170426",
      "code_info": "Batch Numbers: F91770, F92141,  G10378,  G10379, G10788, G10790  G11229,  G11230, G11235, G11236, G15938, G15939, G18830, G18832  G27835, G27835, G27836,  G30217, G30218, G30250, G30251, G32170"
    }
  ]
}