{
  "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": [
    {
      "country": "United States",
      "city": "Haltom City",
      "address_1": "4620 N Beach St",
      "reason_for_recall": "Medtronic Powered Surgical Solutions testing of the Sagittal Saw Rocker Arm Seal identified a potential for leakage of fluid into the motor during use.",
      "address_2": "",
      "product_quantity": "368 devices",
      "code_info": "All Serial Numbers.",
      "center_classification_date": "20160628",
      "distribution_pattern": "Worldwide Distribution-Including the states of AL, AR, AZ, CA, CT, FL, GA, IA, ID, IL, IN, MA, MD, NC, NH, NY, SC, TN, TX, and UT.",
      "state": "TX",
      "product_description": "Saw Sagittal Catalog Number: ES 300; Saw Sagittal Refurbished Catalog Number: ES300-R; Saw Saggital, Finger Catalog Number: ES310; Saw Saggital, Finger Refurbished Catalog Number: ES310-R; Used to dissect bone in surgical applications.",
      "report_date": "20160706",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Sofamor Danek Usa, Inc - Dallas Distribution",
      "recall_number": "Z-2085-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74275",
      "termination_date": "20170613",
      "more_code_info": "",
      "recall_initiation_date": "20160513",
      "postal_code": "76137-3219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}