{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Plantation",
      "address_1": "2555 Davie Rd Ste 110",
      "reason_for_recall": "Stryker Orthpaedics became aware that there is the potential for the 210540 MAKOplasty Hip Array Kit Laminate 150230 to list two part numbers for the RIO Base Array, which is item #5 on the product table.",
      "address_2": "",
      "product_quantity": "10 units.",
      "code_info": "Catalog No. 210540, Lot Code: 150324",
      "center_classification_date": "20160429",
      "distribution_pattern": "CO, KY, MN, WA and WV",
      "state": "FL",
      "product_description": "MAKOplasty Hip Array Kit Laminate 150230",
      "report_date": "20160511",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Mako Surgical Corporation",
      "recall_number": "Z-1588-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73199",
      "termination_date": "20160825",
      "more_code_info": "",
      "recall_initiation_date": "20151125",
      "postal_code": "33317-7424",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}