{
  "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": "92299",
      "recalling_firm": "DeRoyal Industries Inc",
      "address_1": "200 Debusk Ln",
      "address_2": "",
      "postal_code": "37849-4703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of VA.",
      "recall_number": "Z-1692-2023",
      "product_description": "Sterile custom surgical procedure packs    (1) 89-10529.04, CNRV  OR C-SECTION PACK, New River Valley Medical Center; and  (2) 89-10567.05, OB-OR C-SECTION PACK, Carilion Roanoke Memorial Hospital.",
      "product_quantity": "23 cases (52 packs)",
      "reason_for_recall": "The custom procedure packs contain light handle covers that have been recalled by another firm.",
      "recall_initiation_date": "20230417",
      "center_classification_date": "20230607",
      "report_date": "20230614",
      "code_info": "(1) 89-10529.04 - lot 58700691, exp 11/1/2024, GTIN pack-00749756363334, case-50749756363339; (2) 89-10567.05 - lot 58700026, exp 12/1/2024, GTIN pack-00749756364300, case-50749756364305.",
      "more_code_info": ""
    }
  ]
}