{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Englewood",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "89136",
      "recalling_firm": "Denver Solutions, LLC DBA Leiters Health",
      "address_1": "13796 Compark Blvd",
      "address_2": "N/A",
      "postal_code": "80112-7145",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0288-2022",
      "product_description": "Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd, Englewood, CO 80112, (800) 292-6772, NDC 71449-096-42",
      "product_quantity": "1440 vials",
      "reason_for_recall": "Labeling: Label Mix-up: Vials labeled as moxifloxacin 1 mg/mL may actually contain moxifloxacin 5 mg/mL",
      "recall_initiation_date": "20211129",
      "center_classification_date": "20211217",
      "termination_date": "20220712",
      "report_date": "20211229",
      "code_info": "Lot #: 2130958; Expiration Date 03/31/2022"
    }
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}