{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Exeter",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88162",
      "recalling_firm": "Dutch Ophthalmic USA, Inc.",
      "address_1": "10 Continental Dr Bldg 1",
      "address_2": "N/A",
      "postal_code": "03833-7507",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution in the states of AL, CA, CO, FL, MI",
      "recall_number": "Z-2252-2021",
      "product_description": "The device is a 25-gauge infusion line that is part of 25-gauge surgical pack labeled \u001cTDC Vitrectomy Pack VGPC 25g\u001d, Product Number 8525.201.",
      "product_quantity": "16 boxes",
      "reason_for_recall": "Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing 23-gauge infusion line",
      "recall_initiation_date": "20190521",
      "center_classification_date": "20210812",
      "report_date": "20210818",
      "code_info": "Lot Number: 2000401997   Unique Device Identifier (UDI) 08717872021294"
    }
  ]
}