{
  "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": [
    {
      "status": "Terminated",
      "city": "Plantation",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73512",
      "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": "Nationwide Distribution -- AL, CA, CO, CT, FL, GA, IA, ID, IL, IN, LA, MA, MD, MI, MN, MS, NC, NH, NJ, NY, OH, OK, OR, PA, RI, TN, TX, VA, WA, and WI.",
      "recall_number": "Z-1583-2016",
      "product_description": "RESTORIS PST RIO Offset Shell Impactor    For use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.",
      "product_quantity": "96",
      "reason_for_recall": "Potential disassociation of the orientation pin.",
      "recall_initiation_date": "20160223",
      "center_classification_date": "20160428",
      "termination_date": "20161214",
      "report_date": "20160504",
      "code_info": "Lot #'s 28548, 29130, 29479, 30440, 31801, 31802, and 32145."
    }
  ]
}