{
  "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": "86502",
      "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": "Domestic Distribution: CA, CO, CT, GA, IA, IL, IN, MD, MO, NC, NY, OH, PA, SC, TN, TX, WA, WI, WV.    International Distribution: AU, BR, CA, CL, CN, CO, DE, ES, GB, HK, KR, PA, PT, TW.",
      "recall_number": "Z-0301-2021",
      "product_description": "5.5MM Arthrogarde Hip Access Cannula",
      "product_quantity": "143 units",
      "reason_for_recall": "The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.",
      "recall_initiation_date": "20200921",
      "center_classification_date": "20201027",
      "termination_date": "20240322",
      "report_date": "20201104",
      "code_info": "Model: 72201743, Lot: 50838788, 50834909,50846565, 50842905 & 50822169."
    }
  ]
}