{
  "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": "Platteville",
      "state": "WI",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "74878",
      "recalling_firm": "Sperian Eye & Face Protection, Inc",
      "address_1": "825 E Business Highway 151",
      "address_2": "N/A",
      "postal_code": "53818-3763",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide.  Outside the US to include:  Australia, Mexico and United Arab Emirates.",
      "recall_number": "D-0216-2017",
      "product_description": "Honeywell eyesaline Eyewash Sterile Isotonic Solution, sterile water 99%, 32 fl. oz. (946 ml.), Sperian Eye & Face Protection, Inc. (a Honeywell Company), Platteville, WI  53818",
      "product_quantity": "9,744 bottles",
      "reason_for_recall": "Non Sterility; contaminated with Klebsiella pneumoniae",
      "recall_initiation_date": "20160816",
      "center_classification_date": "20161222",
      "termination_date": "20190530",
      "report_date": "20161228",
      "code_info": "Lot number:  F16091-61, exp 03/2019    Product Codes:  32-000455-0000-H5, 32-000455-0036, 32-000461-0036, 32-000462-0000-H5, 32-000462-0036"
    }
  ]
}