{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Billings",
      "state": "MT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76774",
      "recalling_firm": "Windstone Medical Packaging, Inc.",
      "address_1": "1602 4th Ave N",
      "address_2": "N/A",
      "postal_code": "59101-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution including CA, CO, FL, GA, IA, KY, MA, MN, MO, ND, NJ, NV, OH, SD, TX, UT, WI, and WY.",
      "recall_number": "Z-1784-2017",
      "product_description": "Cataract Kit - Dr. Slingsby, part number CMP1017(B.  Product packaged in a convenient manner for use in a general clinical procedure",
      "product_quantity": "990 kits",
      "reason_for_recall": "AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.",
      "recall_initiation_date": "20170316",
      "center_classification_date": "20170411",
      "termination_date": "20170606",
      "report_date": "20170419",
      "code_info": "Lot numbers:    77429  79999  81143  81960  84055  84556  85169  85550  86501  87632  87819  96056  96963  97873  98741  99416  99763  100278  101449",
      "more_code_info": ""
    }
  ]
}