{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87717",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "150 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1031",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the state of FL and the countries of Australia, Japan.",
      "recall_number": "Z-1510-2021",
      "product_description": "CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of soft tissue grafts in anterior cruciate ligament reconstruction, Part Number: 014208",
      "product_quantity": "2 units US and 193 units OUS. 195 units WW",
      "reason_for_recall": "Mislabeled box contained  a 6mm x 20mm screw instead of  6mm x 30mm screw",
      "recall_initiation_date": "20210408",
      "center_classification_date": "20210429",
      "termination_date": "20220622",
      "report_date": "20210505",
      "code_info": "Lot Number: 50906647",
      "more_code_info": ""
    }
  ]
}