{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Vernon Hills",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78369",
      "recalling_firm": "Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company",
      "address_1": "330 Corporate Woods Pkwy",
      "address_2": "N/A",
      "postal_code": "60061-3107",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "IA, WI",
      "recall_number": "D-0160-2018",
      "product_description": "Sterile Eyewash (sterile isotonic phosphate buffered saline solution), 32 oz. 12 units per box. Manufactured by Medex Cardio-Pulmonary Inc. d.b.a. Smiths Medical Company, 300 Corporate Woods Pkwy, Vernon Hills. Illinois, USA 60061. Model Number: 32-005587",
      "product_quantity": "96,828 32 oz bottles",
      "reason_for_recall": "Lack of sterility assurance:  leaking containers which could lead to exposure to infectious agents.",
      "recall_initiation_date": "20170905",
      "center_classification_date": "20180105",
      "termination_date": "20181219",
      "report_date": "20180117",
      "code_info": "Lot: A257, EXP 05-20-2018; A258, EXP 05-19-2018; B017, EXP 01-12-2019; B116, B119, EXP 05-03-2019; B120, EXP 05-04-2019; B131, EXP 05-05-2019; Z535, EXP 10-13-2017; Z638, EXP 12-19-2017.",
      "more_code_info": ""
    }
  ]
}