{
  "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-1799-2017",
      "product_description": "Vitrectomy Kit, part number CMP1016(A.  Product packaged in a convenient manner for use in a general clinical procedure",
      "product_quantity": "440 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:     75908  78658  79157  79577  81959  83285  84916  85168  86500  87319  88343  88984  89749  96802  99415  102487",
      "more_code_info": ""
    }
  ]
}