{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Davie",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79585",
      "recalling_firm": "Mako Surgical Corporation",
      "address_1": "2555 Davie Rd Ste 110",
      "address_2": "N/A",
      "postal_code": "33317-7424",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, KS, LA, MA, MD, MI, MN, NC, NE, NH, NJ, NY, OK, OR, PA, RI, SC, TX, UT, VA, WA, WY,  and Hawaii  Australia, Italy, Netherlands, Singapore, South Korea, United Kingdom, and   Vietnam",
      "recall_number": "Z-1644-2018",
      "product_description": "RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.",
      "product_quantity": "126",
      "reason_for_recall": "Incorrect product and/or label. Sizing is labeled incorrectly.",
      "recall_initiation_date": "20171201",
      "center_classification_date": "20180504",
      "termination_date": "20201214",
      "report_date": "20180516",
      "code_info": "Size 2 Item # 180612 Lot # 26080317-01 and   Size 7 Item # 180617 Lot # 26150217-01."
    }
  ]
}