{
  "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": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72908",
      "recalling_firm": "Smith & Nephew, Inc., Endoscopy Div.",
      "address_1": "130 Forbes Blvd",
      "address_2": "N/A",
      "postal_code": "02048",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution to the states of :  AK, AL, CA, CO,  FL, IL, IN, MI, NE, NJ, NY, OH, OK, PA, SC, TN and TX., and to the countries of : Austria, Australia, Canada, Dubai, Great Britain, India, Italy, Korea, Malaysia, Netherlands, Portugal, Sweden, Switzerland, Singapore and South Africa.",
      "recall_number": "Z-0700-2016",
      "product_description": "Biosure Ratchet Driver, Product No: 72201888 For delivery and placement of orthopedic screws. Arthroscopic surgical instrument",
      "product_quantity": "9",
      "reason_for_recall": "Driver does not meet specification, oversized. Driver may not be able to be fully inserted into the screw, or screw may become stuck on the driver.",
      "recall_initiation_date": "20130404",
      "center_classification_date": "20160129",
      "termination_date": "20210322",
      "report_date": "20160210",
      "code_info": "Lot Numbers: 50410950 and 50407175",
      "more_code_info": ""
    }
  ]
}