{
  "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": "Terminated",
      "city": "Victor",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90578",
      "recalling_firm": "Turbett Surgical, Inc.",
      "address_1": "668b Phillips Rd Ofc 1",
      "address_2": "N/A",
      "postal_code": "14564-9741",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Nationwide: CO, FL, NC and PA.",
      "recall_number": "Z-1501-2022",
      "product_description": "Turbett Surgical Container, TS1500",
      "product_quantity": "7 units",
      "reason_for_recall": "Devices were subject to unapproved rework processes.",
      "recall_initiation_date": "20220414",
      "center_classification_date": "20220804",
      "termination_date": "20250220",
      "report_date": "20220810",
      "code_info": "UDI-DI (GTIN): 00859464007113; Lot No./Serial No.: 100036/2017061015, 100036/2017061016, 100036/2017061017, 100036/2017061019, 100036/2017061023, 100036/2017061025, 100065/2017121001 and 100081/2018031004."
    }
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}