{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Camden",
      "state": "DE",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98654",
      "recalling_firm": "TANGENT ENDOSCOPY, LLC",
      "address_1": "2140 S Dupont Hwy",
      "address_2": "",
      "postal_code": "19934-1249",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of North Carolina, Arizona, and Nevada.",
      "recall_number": "Z-2209-2026",
      "product_description": "Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers:     (1) TNG4002-IND.   (2) TNG-4007-6pk.",
      "product_quantity": "53 units",
      "reason_for_recall": "Affected devices exhibited fractures at the distal shaft tip without complete detachment.",
      "recall_initiation_date": "20260323",
      "center_classification_date": "20260515",
      "report_date": "20260527",
      "code_info": "(1) Model Number: TNG4002-IND; UDI-DI: (1) 00850061601001; Lot numbers: 2510900, 2512938, and 2601944.  (2) Model Number: TNG-4007-6pk; UDI-DI: 00850061601001; Lot numbers: 2510900, 2512938, and 2601944",
      "more_code_info": ""
    }
  ]
}