{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "San Jose",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82229",
      "recalling_firm": "Leiter's Enterprises, Inc.",
      "address_1": "17 Great Oaks Blvd",
      "address_2": "N/A",
      "postal_code": "95119-1359",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "CA, AZ, MI, NY",
      "recall_number": "D-0518-2019",
      "product_description": "Cefuroxime 10 mg/mL in Sodium Chloride, Intravitreal injection, 1 mL in a 2mL Vial, Ophthalmic Use Only, Office Use Only, Leiter's (800) 292-6772- 17 Great Oaks Blvd., San Jose, CA 95119. NDC: 70360-007-35.",
      "product_quantity": "569 vials",
      "reason_for_recall": "Incorrect Product Formulation; compounded sterile drug reconstituted using sterile water instead of sterile 0.9% Sodium Chloride.",
      "recall_initiation_date": "20190219",
      "center_classification_date": "20190306",
      "termination_date": "20200226",
      "report_date": "20190313",
      "code_info": "Lot # 1811195, Exp. Date: 05/01/19"
    }
  ]
}