{
  "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": "Powell",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92445",
      "recalling_firm": "DeRoyal Industries Inc",
      "address_1": "200 Debusk Ln",
      "address_2": "N/A",
      "postal_code": "37849-4703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2087-2023",
      "product_description": "Custom medical procedure packs labeled as:    a) STURDI STRAINER TRAY STANDARD, REF '89-5014",
      "product_quantity": "40 units",
      "reason_for_recall": "The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.",
      "recall_initiation_date": "20230530",
      "center_classification_date": "20230703",
      "report_date": "20230712",
      "code_info": "a) REF '89-5014, GTIN 50749756217908 (cs), 00749756217903 (unit), ,  Lot Numbers:  58770294"
    }
  ]
}