{
  "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": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77008",
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "address_1": "4100 E Milham Ave",
      "address_2": "N/A",
      "postal_code": "49002-9704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US (nationwide) Distribution to the states of :  CA, CT, GA, IL, IN, MA, MD, NC, OH, PA, TN, and TX.",
      "recall_number": "Z-2071-2017",
      "product_description": "Stryker PROFESS Registration Kit.  The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a PROFESS Patient Tracker, and a PROFESS Adaptor Cable.",
      "product_quantity": "65",
      "reason_for_recall": "Product shipped proximate to or past the expiration date listed on the product label.",
      "recall_initiation_date": "20170310",
      "center_classification_date": "20170511",
      "termination_date": "20170721",
      "report_date": "20170517",
      "code_info": "Lot #202085  Stryker Product Number: 6001-420-000"
    }
  ]
}