{
  "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": "88146",
      "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": "Letter",
      "distribution_pattern": "Nationwide Distribution in the states of CA, FL, MA,  and UT.",
      "recall_number": "Z-2097-2021",
      "product_description": "Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system  Product Code: 7510.ALC",
      "product_quantity": "13 Boxes",
      "reason_for_recall": "Barcode label extended expiration date. Barcode located at the short side of the outer box shows 2025-10-27 when scanned, while the correct expiry date is 2024-10-01",
      "recall_initiation_date": "20210414",
      "center_classification_date": "20210719",
      "report_date": "20210728",
      "code_info": "Lot Number(s) 039406  Unique Device Identifier (UDI) 08717872016122",
      "more_code_info": ""
    }
  ]
}