{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Menlo Park",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91063",
      "recalling_firm": "Intersect ENT, Inc.",
      "address_1": "1555 Adams Dr",
      "address_2": "N/A",
      "postal_code": "94025-1439",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including in the states of NC, IL, KS, OR, WI, TX, FL, MN, WY, UT, NY, CA, NJ, OK, MD, HI, MT, TN, MO, IA, MA, AZ, GA, LA, ID, SC, WA, SD, ND, CO, NV.",
      "recall_number": "Z-0458-2023",
      "product_description": "Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044",
      "product_quantity": "611 units",
      "reason_for_recall": "Sinus Implant product label displays incorrect product information including: \"Straight Delivery System\", with incorrect reference number and UDI-DI.",
      "recall_initiation_date": "20221021",
      "center_classification_date": "20221208",
      "report_date": "20221214",
      "code_info": "REF: 60044, UDI-DI: M927600440, Lot: 22041901"
    }
  ]
}