{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Weston",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90727",
      "recalling_firm": "Mako Surgical Corporation",
      "address_1": "3365 Enterprise Ave",
      "address_2": "",
      "postal_code": "33331-3524",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution was made to IL and AZ.",
      "recall_number": "Z-1735-2022",
      "product_description": "Stryker USB Converter, Polaris Spectra Camera, Catalog #201148,  a component of the Mako  Robotic-Arm Assisted Surgery System.",
      "product_quantity": "2",
      "reason_for_recall": "Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.",
      "recall_initiation_date": "20220808",
      "center_classification_date": "20220909",
      "report_date": "20220921",
      "code_info": "Lot #22041607, UDI-DI (GTIN) 07613327407280.",
      "more_code_info": ""
    }
  ]
}