{
  "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": "Cary",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93229",
      "recalling_firm": "Sage Products Inc",
      "address_1": "3909 3 Oaks Rd",
      "address_2": "N/A",
      "postal_code": "60013-1804",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and Canada",
      "recall_number": "Z-0356-2024",
      "product_description": "stryker Sage PrimaFit External Urine Management System for the Female Anatomy",
      "product_quantity": "174,960 devices",
      "reason_for_recall": "A small percentage of devices in three lots of product may contain a tape with a natural rubber latex adhesive which is not declared on the label",
      "recall_initiation_date": "20231023",
      "center_classification_date": "20231120",
      "report_date": "20231129",
      "code_info": "GTIN 00618029600417, Lot Codes:  93667, 93614, 93613",
      "more_code_info": ""
    }
  ]
}