{
  "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": "80621",
      "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": "All devices were distributed in the US in the following states: AK, AL, AR, AZ, CA, CO, CT, FL, IA, ID, KS, KY, LA, MA, MD, MI, MN, MO, NE, NC, NH, NJ, NY, NV, OH, PA, RI, SC, SD, TN. TX, UT, VA, WA, WI.",
      "recall_number": "Z-2924-2018",
      "product_description": "Stryker Mako Vizadisc Knee Procedure Tracking Kit",
      "product_quantity": "19,906 total devices",
      "reason_for_recall": "Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip Procedure Tracking Kit have the potential to be damaged on the Vizadisc reflective material causing an inability to be detected by the camera.",
      "recall_initiation_date": "20180724",
      "center_classification_date": "20180824",
      "termination_date": "20221011",
      "report_date": "20180905",
      "code_info": "Catalog Number 107120. Lot Numbers 17097K, 17124K, 17129K, 17136K, 17143K, 17103H.    **EXPANSION** Lot Numbers 17007K, 17013K, 17024K, 17035K, 17054K, 16354H."
    }
  ]
}