{
  "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": "Terminated",
      "city": "Exeter",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88153",
      "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": "Visit",
      "distribution_pattern": "Distribution in US states of IL, IN, MO, PA.",
      "recall_number": "Z-2091-2021",
      "product_description": "Disposable Replacement Backflush Brush Needles (23 gauge/0.6mm)-for use in vitreoretinal surgery Product Number: labeled as 1281.B1D,  product is 1281.B1D06",
      "product_quantity": "12 US",
      "reason_for_recall": "Mislabeled: 1281.B1D Disposable Replacement Backflush Brush Needles label states  (20 gauge/0.9 mm) instead of the correct size of 23 gauge/0.6 mm and the correct product code 1281.B1D06",
      "recall_initiation_date": "20210225",
      "center_classification_date": "20210719",
      "termination_date": "20211105",
      "report_date": "20210728",
      "code_info": "Lot Number(s) 3420011396  Unique Device Identifier (UDI) 08717872003757",
      "more_code_info": ""
    }
  ]
}