{
  "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": "2026-07-22",
    "results": {
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    }
  },
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      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
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        ],
        "brand_name": [
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        ],
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        ],
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        ],
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        ],
        "route": [
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        "substance_name": [
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        ],
        "rxcui": [
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        "nui": [
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        "pharm_class_epc": [
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        ],
        "pharm_class_moa": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "93006",
      "recalling_firm": "SUN PHARMACEUTICAL INDUSTRIES INC",
      "address_1": "2 Independence Way",
      "address_2": "",
      "postal_code": "08540-6620",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide wide in the USA",
      "recall_number": "D-1172-2023",
      "product_description": "Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)), Rx only, Manufactured for Sun Pharma Global FZE by: Laboratoire Unither, Coutances, France  NDC 47335-506-96",
      "product_quantity": "69,707 cartons",
      "reason_for_recall": "Subpotent: Out of Specification result observed for low assay",
      "recall_initiation_date": "20230907",
      "center_classification_date": "20230920",
      "termination_date": "20240213",
      "report_date": "20230927",
      "code_info": "Lot# 10026, Lot 10027, Exp. 09/2023.",
      "more_code_info": ""
    }
  ]
}