{
  "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": [
    {
      "country": "United States",
      "city": "Stuart",
      "address_1": "2580 Se Willoughby Blvd",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA.",
      "address_2": "",
      "product_quantity": "316,464 kits",
      "code_info": "Product Number (s): 60010, 40201, 40202, 40203, 40204, 40205, 40206.",
      "center_classification_date": "20140131",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "state": "FL",
      "product_description": "Cornea Coat, Hydroxypropylmethylcellulose, 1.5ml Syringe,  Rx Only. Manufactured by: Insight Instruments, Inc., 2580 SE Willoughby  Blvd., Stuart, FL 34994, USA. Tel: 772-219-9393.",
      "report_date": "20140212",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Insight Instruments, Inc.",
      "recall_number": "D-1056-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "65107",
      "termination_date": "20170502",
      "more_code_info": "",
      "recall_initiation_date": "20130424",
      "postal_code": "34994-4701",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}