{
  "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": "Peachtree Corners",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91124",
      "recalling_firm": "Stradis Medical, LLC dba Stradis Healthcare",
      "address_1": "3025 Northwoods Pkwy",
      "address_2": "N/A",
      "postal_code": "30071-1524",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US nationwide distribution, and Canada.",
      "recall_number": "Z-0521-2023",
      "product_description": "HENRY SCHEIN, BASIC EXTENDED PACK, Item No.570-2890",
      "product_quantity": "25 units",
      "reason_for_recall": "Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.",
      "recall_initiation_date": "20221102",
      "center_classification_date": "20221214",
      "report_date": "20221221",
      "code_info": "UDI/DI (case) H65857028901, UDI/DI (kit)M75257028900, Serial/Lot Numbers:  22262492001"
    }
  ]
}