{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Portage",
      "address_1": "4100 E Milham Ave",
      "reason_for_recall": "Stryker Instruments is voluntarily recalling the single use 2.5MM Aggressive Blade because the line on the affected part (P/N 5290-928-000, Lot #13280CG2) was a straight line without a number scale or logo. The line required for this part number includes a number scale that goes from 1cm \u0013 7cm.",
      "address_2": "",
      "product_quantity": "90 units",
      "code_info": "P/N 5290-628-000, Lot #13280CG2",
      "center_classification_date": "20140320",
      "distribution_pattern": "US Distribution including the states of  NV, CA, WA, TN, OR, SD, ID, IN and CO., and Internationally to Malaysia",
      "state": "MI",
      "product_description": "2.5MM Aggressive Blade  Known as a Sinuscopic Shaver Blade, this device is composed of a metal cutter and plastic drive shaft that goes into a metal housing supported by a plastic hub.   ENT Precision Cutter, Aggressive, ESSxlHUMMER 4, Rx Only    It is used for ENT procedures and functions by means of rotation when adapted to a handpiece and console. Through the rotation, the necessary tissue is resected as required by the user. The blade housing has an etching line guide that starts with a straight line and along with a scale from 1cm to 7cm in 1cm increments that serves the doctor as a guide by indicating how far the device is being introduced into the surgical area.",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "recall_number": "Z-1247-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67775",
      "termination_date": "20140515",
      "more_code_info": "",
      "recall_initiation_date": "20140318",
      "postal_code": "49002-9704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}