{
  "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": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92713",
      "recalling_firm": "Stryker Corporation",
      "address_1": "1941 Stryker Way",
      "address_2": "N/A",
      "postal_code": "49002-9711",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2463-2023",
      "product_description": "SurgiCount+ Software Application-indicated as an adjunctive technology for augmenting the manual process of counting, displaying and recording the number of RFID-tagged absorbent articles used during surgical procedures  Product Code: 0694-002-090;",
      "product_quantity": "57 units",
      "reason_for_recall": "Potential for current software to miscount when scanning in multiple sponge-products from the same unique sponge-pack type",
      "recall_initiation_date": "20230710",
      "center_classification_date": "20230825",
      "report_date": "20230906",
      "code_info": "GTIN 07613327543094  Software Version: 2.1.8 & 2.20"
    }
  ]
}